FDA inspection
Nucletron BV: FDA inspection ending Mar 24, 2016
FDA inspection 962608 · No Action Indicated (NAI) · Veenendaal
Key facts
| Inspection ID | 962608 |
|---|---|
| Firm | Nucletron BV |
| FEI number | 3002807741 |
| Address | Waardgelder 1, POBox 930 |
| City | Veenendaal |
| Country | Netherlands |
| Fiscal year | 2016 |
| Inspection end date | Mar 24, 2016 |
| 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