FDA Inspection 1258469 — Medin Technologies, Inc.

Medin Technologies, Inc. — FEI 3011296511

The FDA completed an inspection of Medin Technologies, Inc. on Jan 16, 2025 in Totowa, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Totowa, NJ (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures