Factory Capability Audit
An on-site assessment of a supplier's equipment, quality systems, workforce and capacity before you commit an order.
Factory Capability Audit, done independently, anywhere in Turkey.
An on-site assessment of a supplier's equipment, quality systems, workforce and capacity before you commit an order. Quality Control TR carries out Factory Capability Audit as part of our wider Audit service line, staffed with engineers whose technical background matches your product category.
Because the value of this service depends on catching the right issues at the right moment, the checklist below is adapted to your specification sheet and approved sample rather than applied as a generic template.
- Production equipment and capacity review
- Quality control process and QC staff assessment
- Scored report benchmarked against your requirements
Who This Is For
Buyers, importers and OEMs sourcing from Turkish factories who need an independent, evidence-based check before committing to or releasing an order.
What You Receive
A structured report with photos, data and a clear recommendation, delivered in English within 24–48 hours of the visit.
What happens, step by step
Agree the audit scope and checklist
Agree the audit scope and checklist with you in advance
Visit the factory for a full-day
Visit the factory for a full-day, on-site assessment
Score capability
Score capability, systems and compliance against the checklist
Deliver a scored report
Deliver a scored report with an approval recommendation
Assessed against recognised methods, not guesswork.
Where applicable, Factory Capability Audit is carried out with reference to ISO 9001 quality management principles, adapted to the specific requirements in your purchase order or specification sheet.
If your buyer, retailer or certification body requires a specific standard not listed here, tell us when you request the service and we will confirm whether it can be accommodated.
Documentation Provided
Photo and video evidence, measurement data, sampling records and a written pass/hold/reject recommendation — formatted so your team can act on it without needing to interpret raw notes.
What this typically catches before it becomes your problem
A representative, not exhaustive, list of the issues audit work in this category most often surfaces.
Missing or informal quality-control documentation and work instructions
Equipment or capacity gaps relative to your required order volume
Calibration records that are expired or cannot be located
Working-hours, wage or safety practices inconsistent with your code of conduct
Sub-contracting to an unapproved second facility without disclosure