
Cover material inspection
Review material identity, color, surface condition and order-specific acceptance points.
Define checkpoints, measurement methods, acceptance criteria and evidence before sample approval and production release.
These views illustrate the workflow stages. A valid project record must identify the applicable model, order, method, acceptance criteria and result.

Review material identity, color, surface condition and order-specific acceptance points.

Confirm the component combination and visible condition before assembly.

Review alignment, fastening and the specified mounting interface.

Measure agreed critical dimensions against the controlled requirement.

Check surface, edge, stitching, symmetry, branding and assembly condition.

Confirm product identification, protection, quantity and approved packing instruction.
This register separates published ChiZe catalog evidence from order-specific records. It prevents a catalog image from being treated as compatibility, inspection or test evidence.
The exact checkpoints depend on the product and buyer requirement. This matrix establishes the minimum structure for project discussion.
Do not infer performance or compliance from a catalog image. Confirm the applicable standard, method, sample, conditions and acceptance criteria before testing.
Evidence is useful only when it is traceable to the product revision and order requirement.
Materials, dimensions, interfaces, appearance, identification and revision.
Sample, drawing, color standard, artwork and packaging reference.
Checkpoint, method, frequency, sample size and acceptance criteria.
Method, conditions, equipment, result, report identity and approval owner.
For seating projects, define the cover, foam, base or shell, rail or bracket, fasteners, color and branding requirements. For drivetrain and brake projects, define the component materials, finish, mating interfaces and operating conditions relevant to the application.
Any REACH, PAHs, Prop 65 or other market-specific requirement must identify its scope, applicable substance list, report expectations and target market during the RFQ review.
Share the product, application, target market, required checks and any applicable test or compliance criteria.