FDA inspection
DENTSPLY Implants (a Division of DENTSPLY IH AB): FDA inspection ending Sep 3, 2009
FDA inspection 613120 · Voluntary Action Indicated (VAI) · Molndal
Key facts
| Inspection ID | 613120 |
|---|---|
| Firm | DENTSPLY Implants (a Division of DENTSPLY IH AB) |
| FEI number | 3002806429 |
| Address | Aminogatan 1 |
| City | Molndal |
| Country | Sweden |
| Fiscal year | 2009 |
| Inspection end date | Sep 3, 2009 |
| 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