FDA Inspection 975781 — Joshua Rovin, MD

Joshua Rovin, MD — FEI 3012229614

The FDA completed an inspection of Joshua Rovin, MD on Jun 15, 2016 in Clearwater, 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
Jun 15, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Clearwater, FL (United States)

Additional Details

Clinical Investigator (CI)