# FDA Inspection 1018230 - Horiba ABX SAS - June 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/7357516e-9b69-4942-a5b6-e78524fefa92
Source feed: FDA_Inspections

> FDA Inspection 1018230 for Horiba ABX SAS on June 29, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018230
- Company Name: Horiba ABX SAS
- Inspection Date: 2017-06-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1018230 - 2017-06-29](https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/a95921d5-8f4c-4ccd-b511-4a1f4f93c1fd)
- [FDA Inspection 851820 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/23221044-95ad-4f76-af39-f5f11757515b)
- [FDA Inspection 851820 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/72e90c46-f407-4424-a688-d0488e875bc0)
- [FDA Inspection 734470 - 2011-06-09](https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/17adb582-47ff-4186-b969-44fde265134a)
- [FDA Inspection 734470 - 2011-06-09](https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/222d825d-b060-4e9c-b880-868d94b69474)

Company: https://www.keypedia.com/companies/horiba-abx-sas/4e7b68b7-a504-4a2d-9bf5-e13e0f3b8dde

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