QUALITY SYSTEM

DEFINED STANDARDS. CONTROLLED RELEASE.

Define the reference, check the product, record the evidence, correct deviations and authorize release against the agreed specification.

ILLUSTRATIVE PROTOTYPE PHOTO · REPLACE WITH VERIFIED LAVYSEN MEDIA

DEFINE

QA defines the standard and prevention process. QC checks the product against the current approved reference.

One controlled production reference

Customer Tech Pack
Style, artwork and construction requirements
Approved PPS
Signed pre-production approval
Golden Sample
Retained physical reference for agreed comparison
Measurement Spec
POM, method, target and tolerance
BOM
Approved fabric, trims and packing components
Version Control
Revision, approver, approval date and change history
Illustrative specification and pattern review
Evidence position: approved specification / PPS record crop. Current image is illustrative; verified record pending.

CHECK

Inspection scope and frequency are agreed for the product, material and production stage.

Incoming quality

Fabric, trims, shade and lot inspection

Illustrative incoming quality

First piece

Initial construction against approved PPS

Illustrative first piece

Inline QC

In-process stitch and appearance checks

Illustrative inline qc

Measurement & fit

Defined POM method and tolerance

Illustrative measurement & fit

Functional testing

Agreed stretch, recovery and durability methods

Illustrative functional testing

Final inspection

Sampling, packing and release decision

Illustrative final inspection

Evidence required: incoming sheet, first-piece approval, line checklist, POM record, scoped test report and final inspection. Images are illustrative until matched to verified records.

Defect grading within the agreed inspection plan

Illustrative critical garment detail

Critical

Safety or applicable compliance risk

Illustrative major garment detail

Major

Function, fit or saleability issue

Illustrative minor garment detail

Minor

Limited appearance deviation

RECORD

A finding should identify the affected order, material and production location.

PO / Style / Lot
Order identity and affected quantity
Line
Production line and inspection stage
Fabric Batch
Fabric Code, color and Dye Lot
Trims Batch
Approved component and supplier batch
QC records
Date, inspector, sample size, findings and disposition
Approval trail
Approved Version, PPS and linked test reports
Illustrative inspection record worktable
Evidence position: redacted PO / lot / line / batch QC record. Verified record pending.

CORRECT

Contain the affected goods, establish the cause and verify the correction before release.

  1. Defect Found

    Record the deviation against the agreed standard

  2. Isolate

    Hold and identify the affected goods

  3. Assess

    Determine scope, severity and disposition

  4. Root Cause

    Review material, method, equipment and handling

  5. Correct

    Apply approved rework or corrective action

  6. Re-inspect

    Check corrected goods and record the result

  7. Update SOP / CAPA

    Carry preventive action into the controlled process

Corrective-action evidence

Reserve the defect photograph, hold tag, root-cause review, rework record and re-inspection result for the same PO and lot. No actual CAPA record has been supplied for publication.

RELEASE

Shipment follows the agreed acceptance plan and an authorized release decision.

Final Inspection
Review workmanship, measurement, assortment, labels and packing
AQL
AQL 2.5 planning reference; level and defect limits agreed by order
Customer Inspection
Access, timing and scope arranged with the buyer
Third-party Inspection
Independent inspection under the agreed sampling plan
Release Authority
Named approver and hold / release status recorded before dispatch
Repeat Order
Carry approved PPS, Fabric Code, QC history and CAPA into a fresh lot review
Supporting quality and certificate records · pending verification

Source of standards: Use the customer's Tech Pack, approved PPS, golden sample, measurement specification and BOM. QC must work from the latest approved revision.

Incoming quality: Inspect Fabric Code, shade, width, GSM, defects and dye lot; inspect elastics, threads, zippers, pads, labels, logos, hangtags and packaging. Hold or reject nonconforming lots and record the disposition.

Cutting and first article: Confirm fabric relaxation, spreading direction, marker and pattern version, cut-part ID and the first article against PPS, POM, logo and packing requirements.

Inline QC: At an agreed production stage, sample seams, skipped stitches, waviness, measurements, logo and symmetry. Define line frequency, reaction, owner and record; stop, rework, adjust and reinspect where needed.

Garment workmanship: Use a visual defect standard for skipped or broken stitches, loose threads, holes, stains, seam waviness, twisting and asymmetry. Inspect high-stretch gusset, waistband, side-seam and strap zones.

Measurements and fit: Measure every defined POM against its own tolerance using a consistent flat or stretched method. Sample multiple sizes; passing dimensions does not replace movement and fit review.

Fabric and functional testing: Specify GSM, shrinkage, colorfastness, pilling, stretch, recovery, conditional opacity, wash and logo durability. The test sample, method, color, GSM and extension must be recorded; third-party testing is available by agreement.

Final inspection: After sufficient bulk completion and packing, check quantity, size, color, workmanship, POM, logo, labels, barcode, assortment and carton marks. Use AQL 2.5 or the buyer's agreed sampling plan; hold, rework, replace or reinspect a rejected lot.

Defect grading: Classify Critical safety or compliance faults, Major function or saleability faults and Minor appearance deviations. Keep an approved photo library for accept / reject decisions.

Traceability and records: Link PO, lot, line, date, fabric and trim batches. Retain incoming, inline, measurement, final and test records against the latest approved PPS and version.

Nonconformance and CAPA: Record and isolate the issue, assess root cause across people, machinery, materials, method and environment, then correct, reinspect and update SOP, checklist or training.

Third-party and buyer participation: Allow agreed buyer QC or third-party on-site or video inspection. Share packing list, size breakdown, standard and PPS reference before inspection; define failed-inspection responsibility and reinspection.

Quality team and authority: Verify QA Manager, inline QC, final QC and lab roles. Define stop-line and stop-shipment authority, training and KPI such as first-pass yield, defect and rework rates before publishing actual values.

Repeat orders and scale: Carry forward the approved Fabric Code, pattern, PPS, BOM, QC standard and prior CAPA. Reconfirm new dye lots and increase inspection resources when output scales.

Certification file: Show OEKO-TEX, BSCI, GRS, SEDEX, WRAP or ISO only if an actual file states number, holder, validity and whether it covers factory, fabric or product. Do not claim blanket US compliance.

Illustrative final garment inspection
Evidence position: signed final inspection and release record. Illustrative image; verified document pending.

REQUEST THE STANDARD BEHIND THE CHECK.

Share the product and inspection scope to review the applicable QC reference.

REQUEST QC STANDARD