If you’re preparing your first inspection in China, you’ve probably asked: What AQL level should I choose? What counts as a failure? Do I need in-line checks or just pre-shipment? This guide explains AQL in plain language, shows how to set acceptance criteria, and gives examples you can copy into a PO—so quality is decided before boxes move, not after a return.
AQL (Acceptable Quality Limit) is a sampling plan and a decision rule. You don’t check every unit; you check a statistically chosen sample. If defects in that sample stay at or below the allowed count, the lot passes. If they exceed it, the lot fails and needs rework, replacement, or re-inspection. AQL prevents endless debates by defining “how many defects are too many” in advance.
Your PO should say which issues fall in each bucket. If you don’t define them, the factory will—on the fly.
Use ANSI/ASQ Z1.4. You pick a general inspection level (II is standard for most orders), find your code letter from the lot size, then read the sample size and the accept/reject numbers for each defect class.
A practical default for first runs:
That mix catches real problems without stalling every ship date. Lower AQL numbers = stricter (fewer defects allowed). Raise them only after consistent performance.
For new suppliers or new SKUs, run both. Once the process is stable, you can lighten DUPRO frequency and keep PSI strict.
Order: 5,000 units
Level: General II (ANSI/ASQ Z1.4)
AQL: CR 0.0 / MA 2.5 / MI 4.0
Checklist: Function ✓, key dimensions ±0.3 mm, finish per sample, label/COO, barcode scans, pack per dieline, drop test 3 edges/1 corner (where applicable).
Golden sample: #GS-042, dated, signed by both parties.
Photos: 20+ across sampling, defects (if any), labeling, carton, pallet.
Outcome: Pass/Fail with counts by defect class; re-inspect after rework if failed.
Put this block in your PO. Everyone then follows the same script.
Example A — Pass: Sample size = 200. Allowed at MA 2.5 is 10 defects; MI 4.0 is 14. Inspector finds 6 MA, 9 MI, 0 CR. Result: Pass. Ship or fix minors at supplier’s discretion.
Example B — Fail: Same sample. Inspector finds 0 CR, 12 MA, 7 MI. Result: Fail (MA exceeds 10). Action: rework/replace items causing MA, re-inspect affected cartons.
Example C — Automatic Fail: Any critical defect (e.g., wrong plug, missing warning label required by law). Result: Fail regardless of MA/MI counts.
If the unit, label, or site says it does something, inspect for that claim. If your lamp claims 90 CRI, have a way to verify. If packaging claims “drop-tested,” the pack should survive your route’s drop equivalent. Most chargebacks come from a claim that no one checked before ship.
A golden sample that lives in someone’s desk is not protection. Treat it like a mini-spec: date it, sign it, photograph it, and refer to it in the checklist. If the supplier wants to change a component, finish, or tolerance—approve a new golden before the line restarts.
Tighten (lower AQL) for life-safety, high return risk, or strict retailers. Relax slightly after several clean runs with the same build and supplier. Don’t toggle per shipment; quality systems hate whiplash.
We don’t treat AQL as paperwork. We set the plan with you, run DUPRO and PSI as the program needs, coordinate lab tests where markets require them, and deliver a same-day report with photos, measurements, and clear pass/fail. Findings flow to our Logistics & Export team so labels, counts, and documents match what inspectors saw—reducing holds and chargebacks.
Next steps: If you need a plan you can paste into your PO today, send your spec, target market, and ship date. We’ll return an AQL line, a checklist tied to your product, and an inspection schedule that fits your build.