FDA Inspection 1024263 — Armando Santoro, MD

Armando Santoro, MD — FEI 3004124536

The FDA completed an inspection of Armando Santoro, MD on August 4, 2017 in Rozzano. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 4, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rozzano (Italy)

Additional Details

Clinical Investigator (CI)