FDA inspection
Vivonic GmbH: FDA inspection ending May 19, 2017
FDA inspection 1017154 · Voluntary Action Indicated (VAI) · Sailauf
Key facts
| Inspection ID | 1017154 |
|---|---|
| Firm | Vivonic GmbH |
| FEI number | 3010850471 |
| Address | Kurfurst-eppstein-ring 4 |
| City | Sailauf |
| Country | Germany |
| Fiscal year | 2017 |
| Inspection end date | May 19, 2017 |
| 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