FDA Inspection 1214788 — Peter W. Blumencranz, M.D.

Peter W. Blumencranz, M.D. — FEI 3027331643

The FDA completed an inspection of Peter W. Blumencranz, M.D. on August 4, 2023 in Clearwater, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 4, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Clearwater, FL (United States)

Additional Details

Clinical Investigator (CI)