FDA inspection
Relitech B.V.: FDA inspection ending May 1, 2025
FDA inspection 1269787 · Voluntary Action Indicated (VAI) · Nijkerk Gld
Key facts
| Inspection ID | 1269787 |
|---|---|
| Firm | Relitech B.V. |
| FEI number | 3014377913 |
| Address | Van Siburgstraat 34 |
| City | Nijkerk Gld |
| Country | Netherlands |
| Fiscal year | 2025 |
| Inspection end date | May 1, 2025 |
| 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