FDA Inspection 1297222 — Emilie Kaczmarek, MD

Emilie Kaczmarek, MD — FEI 3040069159

The FDA completed an inspection of Emilie Kaczmarek, MD on December 5, 2025 in Lille. 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
December 5, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Lille (France)

Additional Details

Clinical Investigator (CI)