FDA Inspection 1239221 — Biorep Technologies, Inc.

Biorep Technologies, Inc. — FEI 3005593675

The FDA completed an inspection of Biorep Technologies, Inc. on Apr 26, 2024 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
Apr 26, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami Lakes, FL (United States)