FDA inspection
INTERVASCULAR, SAS: FDA inspection ending Sep 19, 2019
FDA inspection 1102286 · Voluntary Action Indicated (VAI) · La Ciotat Cedex
Key facts
| Inspection ID | 1102286 |
|---|---|
| Firm | INTERVASCULAR, SAS |
| FEI number | 3002707083 |
| Address | 1 Zone Industrielle Athelia |
| City | La Ciotat Cedex |
| Country | France |
| Fiscal year | 2019 |
| Inspection end date | Sep 19, 2019 |
| 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
- 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