FDA Inspection 1043579 — Biorep Technologies, Inc.
The FDA completed an inspection of Biorep Technologies, Inc. on Feb 5, 2018 in Miami Lakes, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 5, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Miami Lakes, FL (United States)