FDA Inspection 590364 — Advarra IRB
The FDA completed an inspection of Advarra IRB on Jun 4, 2009 in Columbia, MD. 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 4, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Columbia, MD (United States)
Additional Details
IRB