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FDA Inspection 928510 — Richard Harvey, MD

Richard Harvey, MD — FEI 3011569558

The FDA completed an inspection of Richard Harvey, MD on Feb 27, 2015 in Chicago, IL. 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
Feb 27, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources