FDA inspection
EPflex Feinwerktechnik GmbH: FDA inspection ending Sep 19, 2024
FDA inspection 1249545 · Voluntary Action Indicated (VAI) · Dettingen An Der Erms
Key facts
| Inspection ID | 1249545 |
|---|---|
| Firm | EPflex Feinwerktechnik GmbH |
| FEI number | 3003289691 |
| Address | Im Schwollbogen 24 |
| City | Dettingen An Der Erms |
| Country | Germany |
| Fiscal year | 2024 |
| Inspection end date | Sep 19, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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