OUR COMMITMENT TO QUALITY
Quality isn't a department at Atomic Machine — it's built into every step of our manufacturing process. From first article inspection through final delivery, our rigorous quality systems ensure every component meets or exceeds customer requirements.
We're committed to delivering precision machining services for aerospace, defense, medical, and industrial customers that meet or exceed quality requirements, backed by comprehensive certifications, advanced inspection equipment, and decades of experience serving customers with the most demanding requirements.
We continually improve our processes, systems, and capabilities to drive customer success and operational excellence, and our quality systems comply with the certifications and regulatory standards outlined below — including FDA 21 CFR Part 820 for medical device regulation.
OUR QUALITY CERTIFICATIONS
Atomic Machine maintains comprehensive industry certifications and registrations, demonstrating our unwavering commitment to quality, safety, and security across all manufacturing operations.
AS9100D — Certified
Aerospace quality management standard for demanding aerospace and defense applications.
ISO 13485:2016 — Certified
Quality management standard for medical device manufacturing and FDA-regulated applications.
ISO 9001:2015 — Certified
Comprehensive Quality Management System (QMS) for consistency, reliability, and excellent processes
FDA 21 CFR PART 820 — Registered
Our quality system is registered to FDA 21 CFR Part 820 by Perry Johnson Registrars, meeting the U.S. quality system regulation for medical device manufacturing.
SAFETY, SECURITY & COMPLIANCE
Quality extends beyond manufacturing to encompass workplace safety, data security, and regulatory
compliance — protecting our team, our customers, and the sensitive information we handle.
OSHA COMPLIANT
Rigorous workplace safety protocols protecting our team and facility every day.
CMMC LEVEL 1
CYBER SECURITY
Cybersecurity controls that safeguard Federal Contract Information and customer data.
FDA 21 CFR PART 820
Medical device quality system requirements, audited by Perry Johnson Registrars, for full traceability and documented control.
OUR 4-PHASE INSPECTION PROCESS
Quality verification at every stage of manufacturing ensures every component meets specifications before, during, and after production.
PHASE 1
First Article Inspection
Comprehensive verification of the first manufactured
part to confirm all dimensions, tolerances, and
specifications before production begins.
PHASE 2
In-Process Inspection
Continuous monitoring throughout production with
regular sampling — ensuring consistent quality and
catching variations early.
PHASE 3
Capability Studies
Statistical process analysis (Cpk/Ppk) to verify manufacturing consistency and confirm repeatable, predictable results across the full production run.
PHASE 4
Final Inspection
Complete verification of finished components
against specifications using advanced inspection
equipment before shipment.
ADVANCED INSPECTION EQUIPMENT
We invest in the best inspection technology to verify every critical dimension and ensure consistent quality across all manufactured components.
COMPLETE QUALITY DOCUMENTATION
Every project includes the comprehensive documentation required for aerospace, medical, and defense applications — ensuring full traceability and regulatory compliance.
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FAIR (First Article Inspection Reports) Verification documentation for first manufactured part
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PPAP (Production Part Approval Process) Standardized approval process for production parts
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Material certifications
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Process certifications
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Inspection reports
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Full traceability records
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Custom documentation as required