FDA inspection
AMTRION GMBH (Formerly Haseke & Kroemker): FDA inspection ending Dec 11, 2014
FDA inspection 906511 · Voluntary Action Indicated (VAI) · Porta Westfalica
Key facts
| Inspection ID | 906511 |
|---|---|
| Firm | AMTRION GMBH (Formerly Haseke & Kroemker) |
| FEI number | 3005285078 |
| Address | Nordring 27a |
| City | Porta Westfalica |
| Country | Germany |
| Fiscal year | 2015 |
| Inspection end date | Dec 11, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| 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
- 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