FDA inspection
Eurotrol B.V.: FDA inspection ending May 6, 2016
FDA inspection 972348 · Voluntary Action Indicated (VAI) · Ede Gld
Key facts
| Inspection ID | 972348 |
|---|---|
| Firm | Eurotrol B.V. |
| FEI number | 3005695774 |
| Address | Keplerlaan 20 |
| City | Ede Gld |
| Country | Netherlands |
| Fiscal year | 2016 |
| Inspection end date | May 6, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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