# FDA Inspection 1102286 - INTERVASCULAR, SAS - September 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/intervascular-sas/63b93fc0-1ba3-4892-854b-65cfbd5ce180
Source feed: FDA_Inspections

> FDA Inspection 1102286 for INTERVASCULAR, SAS on September 19, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102286
- Company Name: INTERVASCULAR, SAS
- Inspection Date: 2019-09-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102286 - 2019-09-19](https://www.keypedia.com/records/fda_inspections/intervascular-sas/b367dd8d-0a04-4e6d-873e-153f35553cc5)
- [FDA Inspection 931561 - 2015-06-18](https://www.keypedia.com/records/fda_inspections/intervascular-sas/d702f64c-2833-4a5d-bbae-b4d26171ff36)

Company: https://www.keypedia.com/companies/intervascular-sas/b37e8eb2-91cb-45b1-b344-8ae072c41963

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7