FDA inspection
Abbott Laboratories: FDA inspection ending Apr 1, 2011
FDA inspection 716720 · Voluntary Action Indicated (VAI) · Santa Clara, CA
Key facts
| Inspection ID | 716720 |
|---|---|
| Firm | Abbott Laboratories |
| FEI number | 2919069 |
| Address | 4551 Great America Pkwy |
| City | Santa Clara |
| State | CA |
| ZIP | 95054 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Apr 1, 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