FDA Inspection 1302278 — Johanna Wilmink

Johanna Wilmink — FEI 3040625276

The FDA completed an inspection of Johanna Wilmink on December 12, 2025 in Amsterdam. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 12, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Amsterdam (Netherlands)

Additional Details

Clinical Investigator (CI)