FDA inspection
OBERON GmbH Fiber Technologies: FDA inspection ending Oct 13, 2017
FDA inspection 1028572 · Voluntary Action Indicated (VAI) · Wildau
Key facts
| Inspection ID | 1028572 |
|---|---|
| Firm | OBERON GmbH Fiber Technologies |
| FEI number | 3011310540 |
| Address | Freiheitstr. 120 |
| City | Wildau |
| Country | Germany |
| Fiscal year | 2018 |
| Inspection end date | Oct 13, 2017 |
| 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