Quality system evidence
ISO 9001 Underwear Manufacturer: What the Certified QMS Covers
Use certificate 62726Q00153R001 as a supplier-qualification signal within its stated sales-related scope, then define the production and inspection records required for the actual order.


ISO 9001 certifies a quality management system within the scope stated on the certificate. It does not certify the underwear product, guarantee a defect rate or replace the order-specific conformity evidence required for a buyer's product and destination market.
Evidence at a glance
What ISO 9001 Certificate 62726Q00153R001 Covers
The recorded scope is sales-related quality management. Factory, production-line, AQL, test and defect-rate statements need separate evidence.
| Standard | ISO 9001:2015 / GB/T 19001-2016 idt |
|---|---|
| Certificate no. | 62726Q00153R001 |
| Holder | Shenzhen Ljvogues Sports Fashion Ltd |
| Certification body | JingXin Certification (Beijing) Co., Ltd. |
| Issued | 2026-03-02 |
| Valid through | 2029-03-01 |
| Recorded scope | Sales-related quality management for the listed underwear categories |
Original document view
Verify the Holder, Scope and Validity Before Approval
The detail crop keeps the holder, management-system standard, sales-related scope and validity dates readable without changing the original certificate wording.

Evidence boundary
Separate the QMS Certificate from the Order File
The certificate scope names several underwear categories, but each sourcing program still needs its own specification and order records.
Certificate layer
- Certified management-system scope
- Document and responsibility framework
- Third-party assessment of that system
- Current holder and validity
Order evidence layer
- Approved tech pack and specification
- Material and component records
- Agreed inspection and sampling plan
- Test and corrective-action records

Record What OQC Checked for the Actual Order
This photograph shows a finished-garment inspection activity. The order file should still define the sample basis, defect categories, acceptance criteria, findings and disposition.
The inspection photograph supports process context; it is not evidence that every order passed and is not created by the ISO 9001 certificate itself.
Related buyer resources
Match the QMS Scope to the Product Program
The certificate names underwear categories, but each program still needs its own specification, approvals and order records.
Order control
Define the Quality File Before Bulk
“AQL 2.5” alone is not a complete inspection plan; define the full control basis before bulk.
Specify
Lock measurements, materials and construction.
Approve
Confirm the sample and tolerances.
Inspect
Apply the agreed control points.
Record
Keep the required inspection evidence.
Close
Document deviations and actions.
Buyer next step
Turn System Evidence into an Order Quality Plan
Use the sample approval checklist to convert requirements into approval records, then compare them with the factory-audit workflow when evaluating production controls.
Buyer FAQ
FAQ About ISO 9001 and Custom Underwear Orders
Use the system certificate and project quality records for different decisions.
Does ISO 9001 certify the underwear product?
No. ISO 9001 certifies a quality management system within the scope stated on the certificate. Product conformity and order performance require their own specifications, inspections and test records.
Does the certificate prove that production is covered?
The current working certificate summary states a sales-related quality-management scope. Buyers should read the original scope wording and use separate factory, audit and order records when evaluating production controls.
Is AQL 2.5 included automatically?
No. An AQL inspection must be agreed for the order, including the applicable standard, inspection level, sampling plan, defect classification and acceptance criteria.
Can I request quality records before shipment?
Yes, where they are included in the project quality agreement. Define the required material, in-process, final-inspection, test and corrective-action records during quotation rather than assuming they are created by the certificate itself.
Define the quality file
Set the Evidence Required for Your Order
Send the product category, tech pack, destination market and inspection requirements. LJUNDERWEAR can identify the available system evidence and the separate order records to define.
Get Your Free Quote & Technical Review
How To Submit Your RFQ
1.Send product type, quantity, and target market.
2.Attach tech packs, photos, or samples.
3.Get sample, MOQ, cost, and timeline guidance.

