FDA inspection
Abiomed Europe GmbH: FDA inspection ending Jun 23, 2016
FDA inspection 979231 · No Action Indicated (NAI) · Aachen
Key facts
| Inspection ID | 979231 |
|---|---|
| Firm | Abiomed Europe GmbH |
| FEI number | 3007904765 |
| Address | Neuenhofer Weg 3 |
| City | Aachen |
| Country | Germany |
| Fiscal year | 2016 |
| Inspection end date | Jun 23, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Project Evaluation: 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