Quality

Supplier Audit Checklist: What to Check in a Chinese Factory

A ready-to-use checklist for auditing a Chinese factory, organised by category — legal entity and qualifications, capacity and equipment, quality system, incoming material control, process control, inspection capability, environment and safety, and reference customers.

GRDH Precision · October 2026 · 11 min read
Quality control inspection of metal parts in a factory

TL;DR — Key Takeaways

How to Use This Checklist

This checklist is written to be printed and carried. It is organised into eight categories that follow the order material moves through a factory: who the company is, what it can do, how it controls quality, then material, process, inspection, workplace and finally its record with customers. You do not need to be a metallurgist to use it; you need to know what evidence each answer should produce.

Audit the production site, not the meeting room. Ask each question of the person who actually runs that step, and ask to see the record that proves it. If you cannot visit, a documented audit by a third party on the ground substitutes for most of it — our guide to supplier audits in China explains how that is run and what it covers.

The Audit Checklist by Category

The table below is the core of the checklist. For each category it lists the key items to check and the evidence that should satisfy you. Use the third column as your acceptance test: if the evidence exists and matches, the item passes. If it does not exist, note it as a finding rather than assuming the factory does the right thing informally.

CategoryWhat to CheckEvidence That Satisfies You
1. Legal entity & qualificationsBusiness license & unified social credit code; scope includes manufacturing; entity matches the bank account; any industry-specific qualificationsLicense copy, registration extract, certificates with their scope shown
2. Capacity & equipmentCasting/forging/CNC equipment with models and tonnage; heat-treatment furnaces; in-house vs outsourced steps; capacity vs your volumeEquipment list, capacity statement, maintenance records, shop-floor photos
3. Quality systemISO 9001 with scope; documented procedures and work instructions; corrective and preventive action; internal audits and management reviewCertificate, quality manual and procedures, CAPA records, internal audit reports
4. Incoming material controlMaterial certificates to EN 10204 3.1; chemical verification or PMI; approved suppliers; segregation and traceability of stockIncoming inspection records, material certificates, PMI logs, marked stock
5. Process controlWork instructions and parameters; first article approval; heat-treatment records; welding procedures and welder qualification; special processes controlledTravellers or routers, process records, WPS/PQR, heat charts, first-off approval
6. Inspection capabilityFinal inspection against your drawing; calibrated gauges, CMM and instruments; defined sampling, e.g. ISO 2859-1; inspection reports issued per batchInspection reports, calibration certificates, CMM programs, sampling plan
7. Environment & safetyHousekeeping and 5S; extraction of dust and fume; personal protective equipment in use; waste handling; safety recordsEHS policy and records, and direct observation on the walkthrough
8. Reference customersCustomers in a similar industry; projects of comparable complexity; repeat business; contactable referencesCustomer list where permitted, sample projects, references you can contact
Manufacturing process inside a Chinese metal parts factory

What a Good Answer Sounds Like

Legal Entity and Qualifications

On legal entity and qualifications, a good answer is short and documented. The supplier names its licensed legal entity, shows a business license whose scope includes manufacturing, and confirms that the bank account beneficiary matches that name. If your product sits in a regulated field, ask which qualifications apply and see the certificates with their scope — not just a logo on a brochure.

Capacity and Equipment

On capacity and equipment, specificity is the signal. A supplier that can list its furnaces, machine tonnage and CNC configuration, and that knows which processes are in-house and which are outsourced, is telling you it runs the floor itself. Ask what share of its capacity your order would take, and check that the schedule it proposes is consistent with that answer.

Quality System and Material Control

On the quality system and incoming material control, the thread to follow is traceability. Ask to see how a heat number or lot number is recorded when material arrives, how it is verified against the certificate issued to EN 10204 3.1, and how it is carried onto the finished part. A factory that can walk you along that thread — and that keeps material segregated and marked — has the foundation the rest of the audit depends on.

Process Control and Inspection

On process control and inspection, look for the records behind the parts. Work instructions, heat-treatment charts, welding procedures and welder qualification, and first article approval all leave paper. So should inspection: final checks against your drawing, calibrated gauges and CMM programs, and a defined sampling plan such as ISO 2859-1. A structured first-off review belongs here too, and our guide to first article inspection explains what it should contain.

Environment, Safety and References

On environment, safety and references, use your eyes and then your follow-up. Good housekeeping, extracted dust and fume, and workers wearing the right protection are visible within minutes, and a factory that manages them usually applies the same discipline to quality. On references, ask for customers in your industry or projects of similar complexity; a supplier that cannot offer one is either very new or very guarded, and both are worth knowing before you order.

Scoring Findings and Making the Call

An audit produces findings, and findings need a consistent scale. We group them into three tiers. Critical findings are those that put the parts themselves at risk — uncontrolled heat treatment, material that cannot be traced, or inspection that never happened. They stop the order until corrected and verified. Major findings, such as a missing calibration record, an undocumented process or weak incoming inspection, need a corrective action and a re-check before production. Minor findings are housekeeping and documentation tidy-up; record them and confirm improvement on the next order.

The judgement to make is not whether a factory is perfect, because almost none are, but whether the gaps it has could reach your part. A minor gap that never touches your processes is not worth delaying a schedule for; a critical gap in the process that makes your part is not something a discount can fix. When findings need independent verification during production, our quality control and inspection in China service carries the audit through to shipment. For where auditing fits in the wider buying process, see industrial parts sourcing in China.

Two habits make an audit worth the day it takes. First, write findings down as you go, with the evidence you saw and the tier you assigned, so that the report does not drift from what actually happened on the floor. Second, agree a follow-up: who will close each corrective action, by when, and what proof will be accepted. An audit that ends with a list and no owner tends to produce the same findings next year.

Keep the checklist as a living document. Each time you audit a supplier, add the questions that turned out to matter and remove the ones that never did. Over time, your own short list — built from your own failures and near-misses — becomes more useful than any generic template, because it reflects the risks you have actually seen in your product.

How GRDH Precision Helps

GRDH Precision is not a factory — we are a sourcing and quality partner based in China. We run supplier audits against exactly this kind of checklist: verifying the legal entity, assessing capacity and equipment, and reviewing the quality system, material control, process control and inspection records on site. You receive a written findings report with photographs and a severity tier for each gap, so the decision to proceed is yours and it is evidence-based. See our supplier audit and quality inspection services.

Conclusion

A checklist only earns its keep if it changes a decision. Use it to build a picture of the supplier as a system — entity, capacity, quality, material, process, inspection, workplace and track record — and then score what you find so that real risks drive real actions. Do the audit before the order, require corrective actions where they matter, and the order you place will rest on evidence rather than optimism. For more on working with suppliers in China, browse the GRDH blog, and if you are still selecting a supplier, start with how to verify a supplier before ordering.

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Frequently Asked Questions

What is a supplier audit?
A supplier audit is a structured on-site assessment of a factory's ability to make your parts to specification. It covers the legal entity, production capacity and equipment, the quality system, incoming material control, process control, inspection capability, the working environment and the supplier's track record with customers. The output is a written findings report that rates gaps by severity, so you can decide whether to proceed, request corrective actions, or look elsewhere.
How long does a factory audit take?
For a focused audit of one factory, allow most of a working day on site to cover the checklist properly and still see the shop floor in action. Larger suppliers or those running several processes may need more than one day. A remote or document-only review can be shorter, but it covers less. The visit itself is only part of the work; writing the findings report and following up on corrective actions takes additional time.
What is the difference between a supplier audit and a quality inspection?
They answer different questions. A supplier audit asks whether a factory is capable of making your parts reliably, before production starts. A quality inspection asks whether specific parts are correct, usually at or near the end of production. Audits reduce the risk of failure; inspections detect it. The two work best together, because an audit without inspection leaves the finished parts unverified, and inspection without an audit keeps catching problems after the cost has already been incurred.
What documents should I ask a factory to prepare for an audit?
Ask for the records that prove each checklist item: the business license and registration details, the ISO 9001 certificate with its scope, a production equipment list, calibration certificates for gauges and instruments, material certificates issued to EN 10204 3.1 with incoming inspection records, process and heat-treatment records, welding procedures and welder qualifications, first article and final inspection reports, and any customer references. A factory that keeps these to hand usually has a real system.
Can a factory audit be done remotely?
Partly. Legal entity and document checks can be done remotely, and a recorded or live video walkthrough can show layout and housekeeping. But process control, material segregation and the culture of the shop floor are hard to judge through a screen. Where a full visit is not practical, a trusted local third party on site is the practical substitute, and it should still produce a written findings report with photographs.
Which audit findings should stop an order?
Critical findings should stop an order until they are corrected and verified. These are the gaps that reach your part directly: material that cannot be traced, heat treatment that is not controlled or recorded, inspection that never took place, or a special process such as welding run without qualified procedures and operators. Major findings need a corrective action and a re-check before production; minor findings can be logged and confirmed on the next order.