FDA inspection
Abbott Vascular: FDA inspection ending Nov 15, 2017
FDA inspection 1031458 · Voluntary Action Indicated (VAI) · Santa Clara, CA
Key facts
| Inspection ID | 1031458 |
|---|---|
| Firm | Abbott Vascular |
| FEI number | 3004635528 |
| Address | 3200 Lakeside Dr |
| City | Santa Clara |
| State | CA |
| ZIP | 95054 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Nov 15, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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
- 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