FDA Inspection 705264 — Kevin Boylan, M.D.
The FDA completed an inspection of Kevin Boylan, M.D. on Jan 7, 2011 in Jacksonville, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jan 7, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Jacksonville, FL (United States)
Additional Details
Clinical Investigator (CI)