# RICARIMPEX SAS CO. – FDA Inspection, Sep 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/ricarimpex-sas-co/23ada42f-abfb-4426-920a-0ed9005b66c8
Source feed: FDA_Inspections

> FDA inspection 1026687 of RICARIMPEX SAS CO., September 20, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026687
- Company Name: RICARIMPEX SAS CO.
- Inspection Date: 2017-09-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1199963 - 2023-02-28

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/ricarimpex-sas-co/c065f850-4f69-4328-8518-af1b127e3108

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