FDA inspection
Ivoclar Vivadent AG: FDA inspection ending Aug 24, 2016
FDA inspection 988253 · Voluntary Action Indicated (VAI) · Schaan
Key facts
| Inspection ID | 988253 |
|---|---|
| Firm | Ivoclar Vivadent AG |
| FEI number | 3002808636 |
| Address | Benderer Strasse 2 |
| City | Schaan |
| Country | Liechtenstein |
| Fiscal year | 2016 |
| Inspection end date | Aug 24, 2016 |
| 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