FDA Inspection 1070030 — Regis Peffault de Latour, M.D.

Regis Peffault de Latour, M.D. — FEI 3014554396

The FDA completed an inspection of Regis Peffault de Latour, M.D. on September 28, 2018 in Paris Cedex 10. 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
September 28, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Paris Cedex 10 (France)

Additional Details

Clinical Investigator (CI)