FDA inspection
Avantec Vascular Corporation: FDA inspection ending Jan 26, 2023
FDA inspection 1195638 · Voluntary Action Indicated (VAI) · Sunnyvale, CA
Key facts
| Inspection ID | 1195638 |
|---|---|
| Firm | Avantec Vascular Corporation |
| FEI number | 3003524171 |
| Address | 870 Hermosa Ave |
| City | Sunnyvale |
| State | CA |
| ZIP | 94085 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Jan 26, 2023 |
| 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