FDA Inspection 1075566 — Morteza Nadjafi, M.D.

Morteza Nadjafi, M.D. — FEI 3014815042

The FDA completed an inspection of Morteza Nadjafi, M.D. on Dec 13, 2018 in Orlando, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 13, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Orlando, FL (United States)

Additional Details

Clinical Investigator (CI)