FDA Inspection 884382 — Stuart A. Harlin, MD

Stuart A. Harlin, MD — FEI 3008266152

The FDA completed an inspection of Stuart A. Harlin, MD on June 20, 2014 in Pensacola, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 20, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Pensacola, FL (United States)

Additional Details

Clinical Investigator (CI)