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Built for Regulated Industries

ISO 9001 certified quality management systems with full traceability and documentation capabilities for aerospace, medical, and energy sectors.

ISO 9001 Certified

Our quality management system meets ISO 9001:2015 standards for design, development, and manufacturing of precision components.

AS9100 Alignment

Our processes align with AS9100 aerospace quality requirements including configuration management and traceability.

Full Traceability

Complete material traceability, test reports, and certificates of conformance for all regulated industry requirements.

Quality Assurance Processes

Systematic quality control at every stage of manufacturing.

First Article Inspection (FAI)

Complete dimensional inspection per AS9102 requirements with full FAIR documentation package including balloon drawings and measurement data.

In-Process Inspection

Statistical process control (SPC) and in-process verification to maintain tight tolerances throughout production runs.

Final Inspection & Testing

100% final inspection with calibrated precision measuring equipment. Functional testing and verification per customer specifications.

Documentation Package

Certificate of Conformance (C of C), material certifications, test reports, and traceability documentation with every shipment.

Material Verification

Material traceability to mill test reports. Positive material identification (PMI) testing when required. Certified material suppliers.

Continuous Improvement

Root cause analysis, corrective and preventive action (CAPA) processes, and ongoing quality system audits and improvements.

Industry-Specific Quality Requirements

Aerospace & Defense

  • AS9100 aligned processes
  • DFARS compliance capability
  • Configuration management
  • First Article Inspection Reports (FAIR)
  • Material traceability to AMS specs
  • ITAR compliance awareness

Oil & Gas

  • API specifications compliance
  • Material certifications (MTRs)
  • Positive Material Identification (PMI)
  • Pressure testing documentation
  • NACE compliance for corrosive environments
  • Full traceability to raw material

Medical Devices

  • ISO 9001 quality systems
  • Material biocompatibility (when required)
  • Cleanroom packaging available
  • Validation documentation support
  • Design History File (DHF) support
  • Non-implantable device focus

Discuss Your Quality Requirements

Let us know your specific quality, certification, or documentation needs for your project.