FDA Inspection 795468 — Gregg A. Feinerman, MD

Gregg A. Feinerman, MD — FEI 3005546383

The FDA completed an inspection of Gregg A. Feinerman, MD on Aug 10, 2012 in Newport Beach, CA. 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
Aug 10, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newport Beach, CA (United States)

Additional Details

Clinical Investigator (CI)