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FDA Inspection 1010223 — Leonard Girardi, MD

Leonard Girardi, MD — FEI 3013437094

The FDA completed an inspection of Leonard Girardi, MD on April 21, 2017 in New York, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New York, NY (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources