FDA Inspection 830265 — Brown Thomas, MD

Brown Thomas, MD — FEI 3009780584

The FDA completed an inspection of Brown Thomas, MD on Apr 12, 2013 in Ocala, 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
Apr 12, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Ocala, FL (United States)

Additional Details

Clinical Investigator (CI)