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Book the Final Random Inspection when production is finished and at least 80% of the goods are packed.
Check these points before the inspection date:
A 10,000-piece order is not ready just because 10,000 pieces appear on the production record. If 1,500 pieces are still being assembled, or one SKU is stored at another location, the finished lot available for inspection is incomplete.
The same problem happens with packing. If only 40% of the goods are packed, carton quantities, assortment, retail packaging, labels, shipping marks, and final pack-out cannot be checked across a properly prepared shipment.
Give each SKU its own quantity and packaging reference. Don’t send only the total order quantity.
| SKU | Model | Variant | Order Qty | Barcode | Packaging |
|---|---|---|---|---|---|
| A01 | Model A | Black / M | 1,000 | Code A01 | Rev. C |
| A02 | Model A | Blue / M | 800 | Code A02 | Rev. C |
| B01 | Model B | Black / L | 1,200 | Code B01 | Rev. B |
The three rows above total 3,000 units. That total can still be correct while the order is wrong. If A01 has 1,100 pieces and A02 has only 700, the shipment still contains 3,000 pieces, but the SKU quantities do not match the order.
Use the same list to connect each SKU with:
This matters even more on mixed orders. Six models sold in four colors can create 24 product combinations before size, plug type, or market version is added.
If an earlier During Product Inspection found a wrong label, loose fitting, missing accessory, or dimension problem, put that item on the FRI recheck list after the factory says it has been corrected.
Send one approved version. Don’t leave three specifications, two artwork files, and an old sample in the inspection folder and expect the inspection team to pick the right one.
| File | Use During FRI |
|---|---|
| Purchase order | SKU, quantity, model and assortment |
| Product specification | Material, components, function and workmanship |
| Drawing / size chart | Dimensions and tolerances |
| Approved sample | Agreed appearance, color, construction or workmanship |
| Packaging artwork | Print, label, barcode, model information and warning text |
| Inspection instruction | AQL, defect rules, test method and special checks |
If the sample has a black screw but the latest specification says silver, settle that before FRI. We should not guess which version the buyer wants.
The same rule applies when something changed after sample approval. A first sample may use one zipper, adapter, fabric, screw, cable, insert, or carton. If another version was later approved for mass production, write that change into the final file.
Also state what the approved sample is approved for. A sample may be:
A sample approved for color is not automatically the standard for every dimension, component, or function.
When the physical sample still needs approval before bulk production, Sample Evaluation can be used to compare it with the drawing, specification, function, and packing requirements earlier in the order.
Write numbers, not phrases such as “normal size,” “good weight,” or “correct length.”
| Check | Example Requirement |
|---|---|
| Overall width | 500 ± 3 mm |
| Cable length | ≥ 1.5 m |
| Hole spacing | 80 ± 1 mm |
| Net weight | 450 ± 10 g |
These numbers are examples, not UTS acceptance limits. Use the tolerances from the buyer-approved drawing, specification, product standard, or other agreed file.
If a drawing says 500 mm but gives no tolerance, we can record an actual result such as 498 mm. We should not decide that ±3 mm is acceptable unless an approved requirement says so.
For a drawing with 30 or 40 dimensions, mark the ones that matter most during FRI. Typical priorities include:
A five-minute measurement that checks an important assembly point is more useful than spending the same time on a dimension that has no effect on fit, function, or buyer acceptance.
“Function test: pass” is too vague. Write down what the product must actually do.
For each special on-site test, give us:
For a timer, for example, the instruction could require the unit to power on, accept a time setting, count down, sound the alarm, and reset correctly. That gives five clear points instead of one vague instruction.
An assembly test needs the same level of detail. State which parts are assembled, which tools are used, and what to check after assembly: fit, alignment, stability, fastening, movement, or function.
Keep factory-site inspection separate from laboratory testing. ISO/IEC 17020:2026 sets requirements for bodies performing inspection.[1] ISO/IEC 17025:2017 applies to testing and calibration laboratories.[2]
Chemical composition, restricted substances, some electrical safety tests, flammability, endurance, and other controlled tests may need laboratory methods instead of a short on-site check. Our article on product testing and product inspection shows where the two scopes differ.
Set the lot size, inspection level, AQL values, and defect categories before FRI.
ISO 2859-1:2026 covers acceptance sampling plans for inspection by attributes and uses Acceptance Quality Limit (AQL) to index the sampling schemes.[3] ANSI/ASQ Z1.4 is also widely used for attribute sampling and includes normal, tightened, and reduced plans.[4]
Before the inspection, confirm:
Here is the example used in the UTS ANSI Sampling Tables:
| Input | Example |
|---|---|
| Lot size | 4,000 units |
| Inspection level | General Inspection Level II |
| Code letter | L |
| Main sample | 200 units |
| AQL example | 2.5 |
| Acceptance number | 10 |
| Rejection number | 11 |
So a buyer should not simply write “check 20 pieces” for that 4,000-unit example. Under the stated plan, the main sample is 200 units.
At AQL 2.5 in this example, 10 is the acceptance number and 11 is the rejection number for the 200-unit sample. That does not mean “2.5% of the whole order may be defective.” AQL works together with the sampling table.
Decide what counts as critical, major, and minor before the result is known.
| Class | Typical Use |
|---|---|
| Critical | A condition that meets the buyer's defined critical rule, often involving a serious safety or other unacceptable risk |
| Major | A defect that can affect function, durability, assembly, important appearance, saleability, or a key specification |
| Minor | A lower-level appearance or workmanship issue that normally does not stop intended use |
The product decides the context. A loose decorative trim and a loose structural part are not the same problem. A small mark under a product and a large mark across the main visible surface are not the same either.
Use a product-specific defect list when you already know where problems happen. For example:
If one condition is unacceptable at any frequency under the buyer's rules, write that clearly instead of leaving it inside a normal cosmetic AQL limit.
A 200-unit AQL sample does not mean every test needs 200 pieces.
| Check | What to Set |
|---|---|
| Workmanship | Main AQL sample |
| Dimensions | Measurement items and sample quantity |
| Function | Method, quantity and expected result |
| Assembly | Quantity and assembly steps |
| Destructive test | Approved quantity and method |
| Packaging | Units and cartons to check |
A destructive test may use only a few samples because the tested units cannot be sold afterward. A basic function check may use another agreed quantity. Measurements may focus on a smaller set of units and several important dimensions.
Write these quantities before inspection. Otherwise a buyer may expect 200 function tests while the working instruction only calls for a much smaller sample.
If every unit must be checked for the agreed points, that is not a normal random-sampling FRI. Depending on the order, a Full Inspection may fit that requirement better.
Match each SKU to the correct product label, retail pack, inner pack, and master carton.
| Level | Check Against |
|---|---|
| Product | Model, product label, rating information and markings |
| Retail pack | Box or bag, manual, accessories, insert, label and barcode |
| Inner pack | Quantity, assortment, divider and inner label |
| Master carton | Quantity, SKU, carton number, shipping mark and packing method |
Useful files include:
Keep only the active version. If Rev. C was approved on August 20, an old Rev. A file should not sit beside it with no status mark.
Watch for cross-SKU errors. A correct Model A product can still have the wrong Model B retail box, Model C manual, or Model D barcode.
Count the assortment, not just the total.
Example: one carton contains 100 pieces and the approved mix is:
If the carton actually contains 40 black, 20 white, 20 blue, and 20 red, it still has 100 pieces. The carton count is right; the assortment is wrong.
Here is another simple example. An order has 100 cartons with 24 units per carton, so the expected packed quantity is 2,400 units. If five cartons contain only 23 units, the shipment is five units short even though all 100 cartons are present.
Use the same check for:
Accessory lists need exact quantities too. If one retail box should contain one main unit, one adapter, one cable, one manual, and one accessory kit, list all five items. A product can work perfectly and still be packed incorrectly.
For master cartons, provide the approved requirements for:
If a carton drop test is required, define the method and sample quantity before inspection.
For barcode or QR-code checks included in the FRI scope, the checked samples need a 100% scan-success rate.
We check three things:
GS1 lists print quality, contrast, damage, position, and packaging interference among the common reasons a barcode may not scan properly.[5]
If 39 of 40 checked barcodes scan, that is 97.5%. It is still not 100%. The unreadable code should be recorded, corrected, and rechecked according to the buyer's requirement.
Routine UTS product inspection does not use barcode grading or scoring as the normal acceptance method. We check whether it is clearly printed, whether it scans, and whether the returned data is correct.
No approved requirement, no invented limit.
For example, a measured length of 498 mm against a 500 mm target is a recorded difference. Without an approved tolerance, it should not automatically become a “failed dimension” based on a limit we created ourselves.
The same applies to labels. If the actual carton says “Model A” but no approved carton artwork was supplied, the report can show what was found; it should not claim the mark matches a file that was never available.
Keep the working FRI pack short and current.
| File | What to Include |
|---|---|
| PO + SKU list | Quantity by model, color, size and version |
| Product specification | Material, construction, dimensions, function and tolerance |
| Approved sample record | What the sample is approved to represent |
| AQL instruction | Inspection level, AQL values and defect rules |
| Test instruction | Method, quantity, result and equipment |
| Packaging artwork | Final box, label, manual, insert and warning files |
| Barcode list | Correct barcode matched to each SKU |
| Packing requirement | Assortment, accessories, carton quantity and carton marks |
| Recheck list | Problems corrected during sample approval, IPI, DPI or earlier production |
Our office team reviews these requirements before arranging the inspection. After FRI, our team provides the recorded sample findings, defect counts, photos, measurements, agreed test results, barcode findings, and packing checks for buyer review.
If the order needs correction after FRI, the next check should focus on what was changed. A buyer dealing with a failed FRI can use a defined recheck or full-inspection plan instead of repeating the same inspection without a clear corrective scope.
Before FRI, check four numbers first: production should be 100% complete, at least 80% should be packed, the lot quantity should match the PO, and each SKU quantity should add up to the total. Then lock the final specification, tolerances, AQL settings, test quantities, artwork, barcode list, and carton rules. In the UTS AQL example, a 4,000-unit lot at General Inspection Level II gives a 200-unit main sample; other tests can use different agreed quantities. If barcode verification is included, all checked codes must scan successfully. Any missing requirement should be recorded as missing, not replaced with a rule made up during inspection.
For a Final Random Inspection (FRI), have the order 100% produced and at least 80% packed. Send one final set of files: the PO and SKU list, product specification, approved sample details, AQL and defect rules, test instructions, packaging artwork, barcode data, and carton requirements. For example, a 4,000-unit lot at General Inspection Level II gives a 200-unit main sample in the UTS AQL table. If barcode verification is included, every checked barcode must scan successfully.
Book the Final Random Inspection when production is finished and at least 80% of the goods are packed.
Check these points before the inspection date:
A 10,000-piece order is not ready just because 10,000 pieces appear on the production record. If 1,500 pieces are still being assembled, or one SKU is stored at another location, the finished lot available for inspection is incomplete.
The same problem happens with packing. If only 40% of the goods are packed, carton quantities, assortment, retail packaging, labels, shipping marks, and final pack-out cannot be checked across a properly prepared shipment.
Give each SKU its own quantity and packaging reference. Don’t send only the total order quantity.
| SKU | Model | Variant | Order Qty | Barcode | Packaging |
|---|---|---|---|---|---|
| A01 | Model A | Black / M | 1,000 | Code A01 | Rev. C |
| A02 | Model A | Blue / M | 800 | Code A02 | Rev. C |
| B01 | Model B | Black / L | 1,200 | Code B01 | Rev. B |
The three rows above total 3,000 units. That total can still be correct while the order is wrong. If A01 has 1,100 pieces and A02 has only 700, the shipment still contains 3,000 pieces, but the SKU quantities do not match the order.
Use the same list to connect each SKU with:
This matters even more on mixed orders. Six models sold in four colors can create 24 product combinations before size, plug type, or market version is added.
If an earlier During Product Inspection found a wrong label, loose fitting, missing accessory, or dimension problem, put that item on the FRI recheck list after the factory says it has been corrected.
Send one approved version. Don’t leave three specifications, two artwork files, and an old sample in the inspection folder and expect the inspection team to pick the right one.
| File | Use During FRI |
|---|---|
| Purchase order | SKU, quantity, model and assortment |
| Product specification | Material, components, function and workmanship |
| Drawing / size chart | Dimensions and tolerances |
| Approved sample | Agreed appearance, color, construction or workmanship |
| Packaging artwork | Print, label, barcode, model information and warning text |
| Inspection instruction | AQL, defect rules, test method and special checks |
If the sample has a black screw but the latest specification says silver, settle that before FRI. We should not guess which version the buyer wants.
The same rule applies when something changed after sample approval. A first sample may use one zipper, adapter, fabric, screw, cable, insert, or carton. If another version was later approved for mass production, write that change into the final file.
Also state what the approved sample is approved for. A sample may be:
A sample approved for color is not automatically the standard for every dimension, component, or function.
When the physical sample still needs approval before bulk production, Sample Evaluation can be used to compare it with the drawing, specification, function, and packing requirements earlier in the order.
Write numbers, not phrases such as “normal size,” “good weight,” or “correct length.”
| Check | Example Requirement |
|---|---|
| Overall width | 500 ± 3 mm |
| Cable length | ≥ 1.5 m |
| Hole spacing | 80 ± 1 mm |
| Net weight | 450 ± 10 g |
These numbers are examples, not UTS acceptance limits. Use the tolerances from the buyer-approved drawing, specification, product standard, or other agreed file.
If a drawing says 500 mm but gives no tolerance, we can record an actual result such as 498 mm. We should not decide that ±3 mm is acceptable unless an approved requirement says so.
For a drawing with 30 or 40 dimensions, mark the ones that matter most during FRI. Typical priorities include:
A five-minute measurement that checks an important assembly point is more useful than spending the same time on a dimension that has no effect on fit, function, or buyer acceptance.
“Function test: pass” is too vague. Write down what the product must actually do.
For each special on-site test, give us:
For a timer, for example, the instruction could require the unit to power on, accept a time setting, count down, sound the alarm, and reset correctly. That gives five clear points instead of one vague instruction.
An assembly test needs the same level of detail. State which parts are assembled, which tools are used, and what to check after assembly: fit, alignment, stability, fastening, movement, or function.
Keep factory-site inspection separate from laboratory testing. ISO/IEC 17020:2026 sets requirements for bodies performing inspection.[1] ISO/IEC 17025:2017 applies to testing and calibration laboratories.[2]
Chemical composition, restricted substances, some electrical safety tests, flammability, endurance, and other controlled tests may need laboratory methods instead of a short on-site check. Our article on product testing and product inspection shows where the two scopes differ.
Set the lot size, inspection level, AQL values, and defect categories before FRI.
ISO 2859-1:2026 covers acceptance sampling plans for inspection by attributes and uses Acceptance Quality Limit (AQL) to index the sampling schemes.[3] ANSI/ASQ Z1.4 is also widely used for attribute sampling and includes normal, tightened, and reduced plans.[4]
Before the inspection, confirm:
Here is the example used in the UTS ANSI Sampling Tables:
| Input | Example |
|---|---|
| Lot size | 4,000 units |
| Inspection level | General Inspection Level II |
| Code letter | L |
| Main sample | 200 units |
| AQL example | 2.5 |
| Acceptance number | 10 |
| Rejection number | 11 |
So a buyer should not simply write “check 20 pieces” for that 4,000-unit example. Under the stated plan, the main sample is 200 units.
At AQL 2.5 in this example, 10 is the acceptance number and 11 is the rejection number for the 200-unit sample. That does not mean “2.5% of the whole order may be defective.” AQL works together with the sampling table.
Decide what counts as critical, major, and minor before the result is known.
| Class | Typical Use |
|---|---|
| Critical | A condition that meets the buyer's defined critical rule, often involving a serious safety or other unacceptable risk |
| Major | A defect that can affect function, durability, assembly, important appearance, saleability, or a key specification |
| Minor | A lower-level appearance or workmanship issue that normally does not stop intended use |
The product decides the context. A loose decorative trim and a loose structural part are not the same problem. A small mark under a product and a large mark across the main visible surface are not the same either.
Use a product-specific defect list when you already know where problems happen. For example:
If one condition is unacceptable at any frequency under the buyer's rules, write that clearly instead of leaving it inside a normal cosmetic AQL limit.
A 200-unit AQL sample does not mean every test needs 200 pieces.
| Check | What to Set |
|---|---|
| Workmanship | Main AQL sample |
| Dimensions | Measurement items and sample quantity |
| Function | Method, quantity and expected result |
| Assembly | Quantity and assembly steps |
| Destructive test | Approved quantity and method |
| Packaging | Units and cartons to check |
A destructive test may use only a few samples because the tested units cannot be sold afterward. A basic function check may use another agreed quantity. Measurements may focus on a smaller set of units and several important dimensions.
Write these quantities before inspection. Otherwise a buyer may expect 200 function tests while the working instruction only calls for a much smaller sample.
If every unit must be checked for the agreed points, that is not a normal random-sampling FRI. Depending on the order, a Full Inspection may fit that requirement better.
Match each SKU to the correct product label, retail pack, inner pack, and master carton.
| Level | Check Against |
|---|---|
| Product | Model, product label, rating information and markings |
| Retail pack | Box or bag, manual, accessories, insert, label and barcode |
| Inner pack | Quantity, assortment, divider and inner label |
| Master carton | Quantity, SKU, carton number, shipping mark and packing method |
Useful files include:
Keep only the active version. If Rev. C was approved on August 20, an old Rev. A file should not sit beside it with no status mark.
Watch for cross-SKU errors. A correct Model A product can still have the wrong Model B retail box, Model C manual, or Model D barcode.
Count the assortment, not just the total.
Example: one carton contains 100 pieces and the approved mix is:
If the carton actually contains 40 black, 20 white, 20 blue, and 20 red, it still has 100 pieces. The carton count is right; the assortment is wrong.
Here is another simple example. An order has 100 cartons with 24 units per carton, so the expected packed quantity is 2,400 units. If five cartons contain only 23 units, the shipment is five units short even though all 100 cartons are present.
Use the same check for:
Accessory lists need exact quantities too. If one retail box should contain one main unit, one adapter, one cable, one manual, and one accessory kit, list all five items. A product can work perfectly and still be packed incorrectly.
For master cartons, provide the approved requirements for:
If a carton drop test is required, define the method and sample quantity before inspection.
For barcode or QR-code checks included in the FRI scope, the checked samples need a 100% scan-success rate.
We check three things:
GS1 lists print quality, contrast, damage, position, and packaging interference among the common reasons a barcode may not scan properly.[5]
If 39 of 40 checked barcodes scan, that is 97.5%. It is still not 100%. The unreadable code should be recorded, corrected, and rechecked according to the buyer's requirement.
Routine UTS product inspection does not use barcode grading or scoring as the normal acceptance method. We check whether it is clearly printed, whether it scans, and whether the returned data is correct.
No approved requirement, no invented limit.
For example, a measured length of 498 mm against a 500 mm target is a recorded difference. Without an approved tolerance, it should not automatically become a “failed dimension” based on a limit we created ourselves.
The same applies to labels. If the actual carton says “Model A” but no approved carton artwork was supplied, the report can show what was found; it should not claim the mark matches a file that was never available.
Keep the working FRI pack short and current.
| File | What to Include |
|---|---|
| PO + SKU list | Quantity by model, color, size and version |
| Product specification | Material, construction, dimensions, function and tolerance |
| Approved sample record | What the sample is approved to represent |
| AQL instruction | Inspection level, AQL values and defect rules |
| Test instruction | Method, quantity, result and equipment |
| Packaging artwork | Final box, label, manual, insert and warning files |
| Barcode list | Correct barcode matched to each SKU |
| Packing requirement | Assortment, accessories, carton quantity and carton marks |
| Recheck list | Problems corrected during sample approval, IPI, DPI or earlier production |
Our office team reviews these requirements before arranging the inspection. After FRI, our team provides the recorded sample findings, defect counts, photos, measurements, agreed test results, barcode findings, and packing checks for buyer review.
If the order needs correction after FRI, the next check should focus on what was changed. A buyer dealing with a failed FRI can use a defined recheck or full-inspection plan instead of repeating the same inspection without a clear corrective scope.
Before FRI, check four numbers first: production should be 100% complete, at least 80% should be packed, the lot quantity should match the PO, and each SKU quantity should add up to the total. Then lock the final specification, tolerances, AQL settings, test quantities, artwork, barcode list, and carton rules. In the UTS AQL example, a 4,000-unit lot at General Inspection Level II gives a 200-unit main sample; other tests can use different agreed quantities. If barcode verification is included, all checked codes must scan successfully. Any missing requirement should be recorded as missing, not replaced with a rule made up during inspection.