# FDA Inspection 949043 - Dilon Technologies France SAS - October 29, 2015

Source: https://www.keypedia.com/records/fda_inspections/dilon-technologies-france-sas/7ea06a2c-eefa-471f-8c2a-86e3d04d824a
Source feed: FDA_Inspections

> FDA Inspection 949043 for Dilon Technologies France SAS on October 29, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 949043
- Company Name: Dilon Technologies France SAS
- Inspection Date: 2015-10-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/dilon-technologies-france-sas/f1278cfd-d85a-4066-969b-6a3c54b69ef7

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