FDA Inspection 1018585 — Patricia Pautier

Patricia Pautier — FEI 3013353648

The FDA completed an inspection of Patricia Pautier on Jun 16, 2017 in Villejuif. 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
Jun 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Villejuif (France)

Additional details

Clinical Investigator (CI)

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