FDA inspection
Abbott Laboratories Inc.: FDA inspection ending Mar 27, 2002
FDA inspection 209300 · No Action Indicated (NAI) · South Pasadena, CA
Key facts
| Inspection ID | 209300 |
|---|---|
| Firm | Abbott Laboratories Inc. |
| FEI number | 2018433 |
| Address | 820 Mission St |
| City | South Pasadena |
| State | CA |
| ZIP | 91030-3142 |
| Fiscal year | 2002 |
| Inspection end date | Mar 27, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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