FDA Inspection 578825 — Missouri Baptist Med Ctr IRB
The FDA completed an inspection of Missouri Baptist Med Ctr IRB on Apr 30, 2009 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
- Apr 30, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Saint Louis, MO (United States)
Additional Details
IRB