FDA Inspection 1242877 — Pieternella S. Lugtenburg

Pieternella S. Lugtenburg — FEI 3030523410

The FDA completed an inspection of Pieternella S. Lugtenburg on May 17, 2024 in Rotterdam. 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
May 17, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rotterdam (Netherlands)

Additional Details

Clinical Investigator (CI)