FDA inspection
EPflex Feinwerktechnik GmbH: FDA inspection ending Feb 26, 2015
FDA inspection 921735 · No Action Indicated (NAI) · Dettingen An Der Erms
Key facts
| Inspection ID | 921735 |
|---|---|
| Firm | EPflex Feinwerktechnik GmbH |
| FEI number | 3003289691 |
| Address | Im Schwollbogen 24 |
| City | Dettingen An Der Erms |
| Country | Germany |
| Fiscal year | 2015 |
| Inspection end date | Feb 26, 2015 |
| Classification | No Action Indicated (NAI) |
| 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