Quality systems & documentation

Define the evidence before production begins.

Applicable quality-system requirements, inspection methods and deliverable records are agreed according to the project, application and customer approval process.

Scope verified

ISO 9001 Quality Environment

Quality-managed production routes can be specified for projects requiring controlled review, production and inspection records.

Project-specific

IATF 16949 Project Alignment

Automotive-oriented quality planning and documentation can be evaluated when the application and sourcing route require it.

Project-specific

ISO 13485 Project Alignment

Medical-device quality requirements can be reviewed during qualification for applicable prototype and component programs.

Scope verified

ISO 14001 Environment

Environmental-management requirements can be included when qualifying a suitable production route.

On request

Material Traceability

Mill certificates, alloy references and treatment records can be included when defined in the order documentation.

On request

Inspection Reporting

FAI, dimensional reports and marked drawings can be agreed before manufacturing release.

Available documentation

Request the records your approval process needs

Certificate of conformity · material certificates · dimensional inspection report · first article inspection · process records · surface-treatment certificates · packaging and export documentation.

Applicable certification status, issuing scope and supporting documents are confirmed privately during technical qualification and before order placement.

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