FDA Inspection 1280386 — 3D Medical Manufacturing, Inc.

3D Medical Manufacturing, Inc. — FEI 3001239363

The FDA completed an inspection of 3D Medical Manufacturing, Inc. on August 15, 2025 in Riviera Beach, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 15, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Riviera Beach, FL (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation
312821 CFR 820.90(a)Nonconforming product control
313021 CFR 820.100(a)Lack of or inadequate procedures
337521 CFR 820.198(e)Records of complaint investigation