# Horiba ABX SAS – FDA Inspection, Jun 9, 2011

Source: https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/222d825d-b060-4e9c-b880-868d94b69474
Source feed: FDA_Inspections

> FDA inspection 734470 of Horiba ABX SAS, June 09, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 734470
- Company Name: Horiba ABX SAS
- Inspection Date: 2011-06-09
- 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: 3

## Related Documents

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- [FDA Inspection 851820 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/72e90c46-f407-4424-a688-d0488e875bc0)

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