FDA Inspection 1035056 — Michael Smith, MD

Michael Smith, MD — FEI 3013730236

The FDA completed an inspection of Michael Smith, MD on Nov 7, 2017 in Phoenix, AZ. 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 7, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)