FDA Inspection 784930 — WakeMed IRB
The FDA completed an inspection of WakeMed IRB on Jun 6, 2012 in Raleigh, NC. 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
- Jun 6, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Raleigh, NC (United States)
Additional Details
IRB