FDA Inspection 643582 — MercyOne North Iowa Medical Center IRB
The FDA completed an inspection of MercyOne North Iowa Medical Center IRB on January 21, 2010 in Mason City, IA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 21, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Mason City, IA (United States)
Additional Details
IRB