FDA Inspection 1018585 — Patricia Pautier

Patricia Pautier — FEI 3013353648

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

Additional Details

Clinical Investigator (CI)