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FDA Inspection 952098 — Arles Perdomo, MD

Arles Perdomo, MD — FEI 3011907319

The FDA completed an inspection of Arles Perdomo, MD on Dec 15, 2015 in Miami, 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 15, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources