FDA Inspection 610574 — Compass IRB, LLC
The FDA completed an inspection of Compass IRB, LLC on Aug 26, 2009 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
- Aug 26, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Mesa, AZ (United States)
Additional Details
IRB