FDA Inspection 966739 — Bridgeport Hospital IRB
The FDA completed an inspection of Bridgeport Hospital IRB on Apr 7, 2016 in Bridgeport, CT. 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 7, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Bridgeport, CT (United States)
Additional Details
IRB