FDA inspection
Nucletron BV: FDA inspection ending May 29, 2008
FDA inspection 528005 · Voluntary Action Indicated (VAI) · Veenendaal
Key facts
| Inspection ID | 528005 |
|---|---|
| Firm | Nucletron BV |
| FEI number | 3002807741 |
| Address | Waardgelder 1, POBox 930 |
| City | Veenendaal |
| Fiscal year | 2008 |
| Inspection end date | May 29, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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