FDA Inspection 837077 — David Mego, MD

David Mego, MD — FEI 3009802801

The FDA completed an inspection of David Mego, MD on June 20, 2013 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
June 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Little Rock, AR (United States)

Additional Details

Clinical Investigator (CI)