FDA inspection
CeramTec GmbH, Medical Products Division: FDA inspection ending Jun 18, 2009
FDA inspection 611270 · No Action Indicated (NAI) · Plochingen
Key facts
| Inspection ID | 611270 |
|---|---|
| Firm | CeramTec GmbH, Medical Products Division |
| FEI number | 3002806653 |
| Address | Building K, CeramTec-Platz 1-9 |
| City | Plochingen |
| Fiscal year | 2009 |
| Inspection end date | Jun 18, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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