The U.S. Food & Drug Administration (FDA) has resumed planning and conducting domestic surveillance inspections across all commodities.
#gmp #fda #regulations #fda21cfrpart820
https://www.fda.gov/news-events/press-announcements/fda-roundup-february-4-2022
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Consulting in: Medical Device, Orthopedic & Spinal Devices, Product Development, Design, 3D CAD,
Engineering, Finite Element Analysis, FEA, Quality Management System, QMS, ISO 13485,
ISO 9001, FDA Compliance, FDA 21 CFR 820, Design History Files & Remediation
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