FDA Inspection 1018449 — James Benjamin Renfroe MD

James Benjamin Renfroe MD — FEI 3013500611

The FDA completed an inspection of James Benjamin Renfroe MD on June 30, 2017 in Gulf Breeze, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 30, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Gulf Breeze, FL (United States)

Additional Details

Clinical Investigator (CI)