FDA Inspection 1243632 — Curium Netherlands B.V.

Curium Netherlands B.V. — FEI 3002806617

The FDA completed an inspection of Curium Netherlands B.V. on June 13, 2024 in Petten. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Petten (Netherlands)