Organisation
Roles, reporting lines and responsibility for production and quality may be reviewed for clarity.
Third-party factory audit · China
Review an identified manufacturing facility, its observable workflow, equipment, quality arrangements and available records before relying on supplier capability claims.
Audit findings describe available evidence at the time of the visit. A facility visit does not certify a supplier or guarantee capacity, compliance or future performance.
How it works
Share the facility address, product and production concerns.
Observe agreed processes and available records, subject to access.
Review documented observations, gaps and unanswered questions.
Factory audit scope
Set the questions around your product and sourcing decision. Each point below depends on access and the documents actually available.
Roles, reporting lines and responsibility for production and quality may be reviewed for clarity.
Storage, identification and movement of relevant materials may be observed where accessible.
Work instructions, production steps and in-process checks may be reviewed against the product context.
Relevant machinery, tools, maintenance information and measurement equipment may be observed within scope.
Available inspection, defect, corrective-action or calibration records may be sampled for consistency and relevance.
Storage and identification practices may be observed, but this does not replace sampling and checking the buyer's actual order.
Observed risk indicators
These are examples of possible findings, not claims about any supplier. The report should also make unavailable evidence explicit.
The visited site, company name or stated relationship to the supplier may differ from the information previously provided to the buyer.
Production steps presented as part of the supplier's capability may actually be subcontracted or performed at another location and should be documented as such where evidence is available.
Expected machinery, tools or measurement equipment may not be observable, may appear unsuitable for the stated process or may have an unclear role in current production.
Storage, identification, segregation or movement of materials, work-in-progress or finished goods may show control gaps relevant to the buyer's product risk.
Incoming, in-process, final inspection, defect, corrective-action or calibration records may be unavailable, incomplete or inconsistent with the stated quality process.
Restricted areas, unavailable documents, unanswered questions or unsupported factory statements remain visible so the buyer knows what could not be confirmed.
Audit process
Provide the factory address, products, expected manufacturing steps and any buyer questionnaire or critical risks.
Review relevant production areas, processes, equipment and available records, subject to access and photography permissions.
Distinguish directly observed conditions, documents shown, factory statements and questions that could not be confirmed.
Documented audit findings
Useful factory audit evidence separates direct observations from statements and records, rather than presenting every claim as verified.
Before booking
A factory address and short set of buyer questions are enough to begin discussing the scope.
Buyer questions
No. It documents evidence within an agreed scope. Certification or compliance conclusions require appropriate standards, authority and evidence and should not be implied.
It may record equipment, workflow, staffing functions and available production information. Those observations do not guarantee actual or future capacity without sufficient supporting evidence.
No. Verification focuses on identity and information consistency. An audit goes further into the identified facility, workflow, resources, quality arrangements and records.
Not automatically. An audit assesses facility and process questions. Checking selected order units against specifications requires a product-inspection scope.
You can send a facility address in Zhejiang, Jiangsu, Anhui or another Chinese sourcing region. The audit brief, site access, timing and service availability must be confirmed before booking.
Factory audit inquiry
Share the factory address, product, planned production processes and key quality concerns. We can clarify the audit brief and provide a quote before confirming a visit.
Simple, transparent pricing
Independent product inspections, supplier verification and factory audits. Choose where your on-site service takes place.
$199 USD / person-day
On-site inspection and verification services in Yiwu.
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$249 USD / person-day
On-site services outside Yiwu, including other cities in Zhejiang.
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Please confirm your inspection scope, date and number of person-days with YiwuQC. Payment does not automatically reserve an inspector.
YiwuQC charges $199 per person-day in Yiwu and $249 per person-day elsewhere in China for standard services. One person working one day is one person-day. The total depends on the agreed number of inspectors and working days. Certification and independent laboratory testing are quoted separately.