FDA Inspection 1071893 — Stein Bernardo, MD

Stein Bernardo, MD — FEI 3011063719

The FDA completed an inspection of Stein Bernardo, MD on Oct 26, 2018 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
Oct 26, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Clearwater, FL (United States)

Additional Details

Clinical Investigator (CI)