FDA Inspection 649224 — Lutheran Hospital IRB
The FDA completed an inspection of Lutheran Hospital IRB on Feb 23, 2010 in Fort Wayne, IN. 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
- Feb 23, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Fort Wayne, IN (United States)
Additional Details
IRB