FDA inspection
Abbott Laboratories: FDA inspection ending Nov 17, 2004
FDA inspection 355370 · Santa Clara, CA
Key facts
| Inspection ID | 355370 |
|---|---|
| Firm | Abbott Laboratories |
| FEI number | 2919069 |
| Address | 4551 Great America Pkwy |
| City | Santa Clara |
| State | CA |
| ZIP | 95054-1208 |
| Fiscal year | 2005 |
| Inspection end date | Nov 17, 2004 |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| Product type | Devices |
At a glance
- None Citations
- None 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