ISO 9001 Quality Environment
Quality-managed production routes can be specified for projects requiring controlled review, production and inspection records.
Quality systems & documentation
Applicable quality-system requirements, inspection methods and deliverable records are agreed according to the project, application and customer approval process.
Quality-managed production routes can be specified for projects requiring controlled review, production and inspection records.
Automotive-oriented quality planning and documentation can be evaluated when the application and sourcing route require it.
Medical-device quality requirements can be reviewed during qualification for applicable prototype and component programs.
Environmental-management requirements can be included when qualifying a suitable production route.
Mill certificates, alloy references and treatment records can be included when defined in the order documentation.
FAI, dimensional reports and marked drawings can be agreed before manufacturing release.
Available documentation
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.