# FDA Inspection 1237221 - Ionisos S.A.S. - April 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/ionisos-sas/75f0afe5-3bd8-420e-8fc1-48e29c9943ba
Source feed: FDA_Inspections

> FDA inspection 1237221 of Ionisos S.A.S., April 05, 2024. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1237221
- Company Name: Ionisos S.A.S.
- Inspection Date: 2024-04-05
- 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: 0

## Related Documents

- [FDA Inspection 838583 - 2013-07-03](https://www.keypedia.com/records/fda_inspections/ionisos-sas/18714a57-4048-4066-944b-4f60743f4339)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/ionisos-sas/def8aeba-584d-46ce-b3b6-3d7ddf0a5e50

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