FDA Inspection 701219 — Robert Feezor, MD
The FDA completed an inspection of Robert Feezor, MD on Dec 13, 2010 in Daytona Beach, FL. 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
- Dec 13, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Daytona Beach, FL (United States)
Additional Details
Clinical Investigator (CI)