FDA inspection
Ivoclar Vivadent Manufacturing GmbH: FDA inspection ending Aug 26, 2016
FDA inspection 988687 · No Action Indicated (NAI) · Burs
Key facts
| Inspection ID | 988687 |
|---|---|
| Firm | Ivoclar Vivadent Manufacturing GmbH |
| FEI number | 1000493628 |
| Address | Bremschlstrase 16 |
| City | Burs |
| Country | Austria |
| Fiscal year | 2016 |
| Inspection end date | Aug 26, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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