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FDA Inspection 1056623 — Gregg A. Feinerman, MD

Gregg A. Feinerman, MD — FEI 3005546383

The FDA completed an inspection of Gregg A. Feinerman, MD on May 7, 2018 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
May 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Newport Beach, CA (United States)

Additional Details

Clinical Investigator (CI)

Facility

Other inspections at this facility

FDA data resources