FDA Inspection 1007856 — David Mego, MD

David Mego, MD — FEI 3009802801

The FDA completed an inspection of David Mego, MD on March 31, 2017 in Little Rock, AR. 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
March 31, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Little Rock, AR (United States)

Additional Details

Clinical Investigator (CI)