FDA Inspection 1155777 — Missouri Baptist Med Ctr IRB
The FDA completed an inspection of Missouri Baptist Med Ctr IRB on Oct 8, 2021 in Saint Louis, MO. 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
- Oct 8, 2021
- Fiscal Year
- 2022
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Saint Louis, MO (United States)
Additional Details
IRB