FDA inspection
EUROIMMUN Medizinische Labordiagnostika AG: FDA inspection ending Jan 17, 2018
FDA inspection 1087255 · Voluntary Action Indicated (VAI) · Lubeck
Key facts
| Inspection ID | 1087255 |
|---|---|
| Firm | EUROIMMUN Medizinische Labordiagnostika AG |
| FEI number | 3003268355 |
| Address | Seekamp 31 |
| City | Lubeck |
| Fiscal year | 2018 |
| Inspection end date | Jan 17, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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