FDA inspection
Greiner Bio-One GmbH: FDA inspection ending Jan 30, 2003
FDA inspection 258501 · Voluntary Action Indicated (VAI) · Kremsmunster
Key facts
| Inspection ID | 258501 |
|---|---|
| Firm | Greiner Bio-One GmbH |
| FEI number | 3000974732 |
| Address | Bad Haller Strase 32 |
| City | Kremsmunster |
| Fiscal year | 2003 |
| Inspection end date | Jan 30, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 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