FDA Inspection
Horiba ABX SASHoriba ABX SAS – FDA Inspection, Sep 19, 2013
Record Details
This FDA Inspection record concerns Horiba ABX SAS, with an inspection on September 19, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Horiba ABX SAS
- Inspection Date
- September 19, 2013
- Product Type
- Devices
View Company Profile
ID · 72e90c46-f407-4424-a688-d0488e875bc0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 851820
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Horiba ABX SAS
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 29, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 9, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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