# FDA Inspection 1229622 - Aptar France SAS - February 08, 2024

Source: https://www.keypedia.com/records/fda_inspections/aptar-france-sas/4237e179-638c-494b-bcbb-588085d2d82b
Source feed: FDA_Inspections

> FDA Inspection 1229622 for Aptar France SAS on February 08, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1229622
- Company Name: Aptar France SAS
- Inspection Date: 2024-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 955098 - 2015-12-02](https://www.keypedia.com/records/fda_inspections/aptar-france-sas/d6a8c40f-0fee-451f-8f8a-427681e235f8)
- [FDA Inspection 674410 - 2010-07-01](https://www.keypedia.com/records/fda_inspections/aptar-france-sas/800905f9-2130-4cb3-9ae6-de56d6b03e6d)
- [FDA Inspection 672898 - 2010-07-01](https://www.keypedia.com/records/fda_inspections/aptar-france-sas/1fbc006b-05a9-49ae-b10d-6b5b596ecba2)

Company: https://www.keypedia.com/companies/aptar-france-sas/b349dbdb-c2c3-43dc-9511-f887c9a99ae5

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