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FDA Inspection 992889 — James Gammie, MD

James Gammie, MD — FEI 3012699893

The FDA completed an inspection of James Gammie, MD on Nov 14, 2016 in Baltimore, MD. 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
Nov 14, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources