# INTERVASCULAR, SAS – FDA Inspection, Sep 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/intervascular-sas/b367dd8d-0a04-4e6d-873e-153f35553cc5
Source feed: FDA_Inspections

> FDA inspection 1102286 of INTERVASCULAR, SAS, September 19, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 931561 - 2015-06-18

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

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