FDA Inspection 1272192 — Nucletron BV

Nucletron BV — FEI 3002807741

The FDA completed an inspection of Nucletron BV on May 15, 2025 in Veenendaal. 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
May 15, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Veenendaal (Netherlands)