FDA inspection
Nucletron BV: FDA inspection ending May 15, 2025
FDA inspection 1272192 · No Action Indicated (NAI) · Veenendaal
Key facts
| Inspection ID | 1272192 |
|---|---|
| Firm | Nucletron BV |
| FEI number | 3002807741 |
| Address | Waardgelder 1, 3900 AX VEENENDAAL, P O B O X 930, Pobox 930 |
| City | Veenendaal |
| Country | Netherlands |
| Fiscal year | 2025 |
| Inspection end date | May 15, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data