FDA Inspection 947825 — Ghiath M. Mikdadi, M.D.

Ghiath M. Mikdadi, M.D. — FEI 3011908561

The FDA completed an inspection of Ghiath M. Mikdadi, M.D. on Nov 6, 2015 in Hammond, LA. 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 6, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Hammond, LA (United States)

Additional Details

Clinical Investigator (CI)