# Horiba ABX SAS – FDA Inspection, Jun 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/horiba-abx-sas/a95921d5-8f4c-4ccd-b511-4a1f4f93c1fd
Source feed: FDA_Inspections

> FDA inspection 1018230 of Horiba ABX SAS, June 29, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- 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: 4

## Related Documents

- [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/222d825d-b060-4e9c-b880-868d94b69474)

## Related Officers

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

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