FDA inspection
Abbott Laboratories Diagnostic Division: FDA inspection ending Mar 31, 2000
FDA inspection 21877 · Official Action Indicated (OAI) · North Chicago, IL
Key facts
| Inspection ID | 21877 |
|---|---|
| Firm | Abbott Laboratories Diagnostic Division |
| FEI number | 1451914 |
| Address | Us Route 41, Martin Luther King Dr. |
| City | North Chicago |
| State | IL |
| ZIP | 60064 |
| Fiscal year | 2000 |
| Inspection end date | Mar 31, 2000 |
| 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
- 10–99 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