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FDA Inspection 730555 — Micah Harris, MD

Micah Harris, MD — FEI 3008986608

The FDA completed an inspection of Micah Harris, MD on Jun 9, 2011 in Phoenix, AZ. 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
Jun 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources