FDA Inspection 824619 — Compass IRB, LLC
The FDA completed an inspection of Compass IRB, LLC on Mar 26, 2013 in Mesa, AZ. 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
- Mar 26, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Mesa, AZ (United States)
Additional Details
IRB