FDA inspection
Greiner Bio-One GmbH: FDA inspection ending Oct 25, 2018
FDA inspection 1069716 · Official Action Indicated (OAI) · Kremsmunster
Key facts
| Inspection ID | 1069716 |
|---|---|
| Firm | Greiner Bio-One GmbH |
| FEI number | 3000974732 |
| Address | Bad Haller Strase 32 |
| City | Kremsmunster |
| Country | Austria |
| Fiscal year | 2019 |
| Inspection end date | Oct 25, 2018 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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