FDA inspection
Maquet Cardiopulmonary GmbH: FDA inspection ending Aug 15, 2013
FDA inspection 857072 · Official Action Indicated (OAI) · Hechingen
Key facts
| Inspection ID | 857072 |
|---|---|
| Firm | Maquet Cardiopulmonary GmbH |
| FEI number | 3009649876 |
| Address | Neue Rottenburger Str. 37 |
| City | Hechingen |
| Country | Germany |
| Fiscal year | 2013 |
| Inspection end date | Aug 15, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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