FDA inspection
Abbott Diagnostics Technologies AS: FDA inspection ending Mar 9, 2011
FDA inspection 712676 · Voluntary Action Indicated (VAI) · Oslo
Key facts
| Inspection ID | 712676 |
|---|---|
| Firm | Abbott Diagnostics Technologies AS |
| FEI number | 3003045237 |
| Address | Kjelsasveien 161 |
| City | Oslo |
| Country | Norway |
| Fiscal year | 2011 |
| Inspection end date | Mar 9, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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