FDA Inspection 756666 — ProMedica Health System IRB
The FDA completed an inspection of ProMedica Health System IRB on December 9, 2011 in Toledo, OH. 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
- December 9, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Toledo, OH (United States)
Additional Details
IRB