FDA inspection
Baxter Althin Medical AB: FDA inspection ending Nov 2, 2001
FDA inspection 195026 · Official Action Indicated (OAI) · Ronneby
Key facts
| Inspection ID | 195026 |
|---|---|
| Firm | Baxter Althin Medical AB |
| FEI number | 3001267558 |
| Address | Box 39, Fridhemsvagen 15 |
| City | Ronneby |
| Fiscal year | 2002 |
| Inspection end date | Nov 2, 2001 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Med 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