FDA Inspection 1005231 — Annamaria De Pellegrin

Annamaria De Pellegrin — FEI 3013108493

The FDA completed an inspection of Annamaria De Pellegrin on Mar 10, 2017 in Vittorio Veneto. 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 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Vittorio Veneto (Italy)

Additional details

Clinical Investigator (CI)

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