FDA Inspection 628553 — Hunter Newsom, MD
The FDA completed an inspection of Hunter Newsom, MD on Nov 13, 2009 in Sebring, 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
- Nov 13, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Sebring, FL (United States)
Additional Details
Clinical Investigator (CI)