FDA Inspection 1032572 — Mitchell B. Miller, MD

Mitchell B. Miller, MD — FEI 3006851258

The FDA completed an inspection of Mitchell B. Miller, MD on Nov 6, 2017 in Safety Harbor, 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
Nov 6, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Safety Harbor, FL (United States)

Additional Details

Clinical Investigator (CI)