FDA inspection
CeramTec GmbH, Medical Products Division: FDA inspection ending Nov 22, 2002
FDA inspection 251942 · Voluntary Action Indicated (VAI) · Plochingen
Key facts
| Inspection ID | 251942 |
|---|---|
| Firm | CeramTec GmbH, Medical Products Division |
| FEI number | 3002806653 |
| Address | Building K, CeramTec-Platz 1-9 |
| City | Plochingen |
| Fiscal year | 2003 |
| Inspection end date | Nov 22, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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