FDA Inspection 1022533 — Diego Cortinovis

Diego Cortinovis — FEI 3013184706

The FDA completed an inspection of Diego Cortinovis on Mar 16, 2017 in Milan. 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
Mar 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Milan (Italy)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.