FDA Inspection 949384 — Roberto Sotolongo, MD

Roberto Sotolongo, MD — FEI 3011938830

The FDA completed an inspection of Roberto Sotolongo, MD on Nov 20, 2015 in Miami, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 20, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Miami, FL (United States)

Additional Details

Clinical Investigator (CI)