Company
FranceHoriba ABX SAS, Montpellier, France – FDA Inspections
Inspection records and compliance data for Horiba ABX SAS in Montpellier. 3 FDA inspections on record, 1 Form 483, last inspected June 29, 2017.
Company Profile
This profile covers Horiba ABX SAS based in Montpellier, France.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 3
- NAI
- 0
- Form 483s
- 1
- Warning letters
- 0
First inspected June 9, 2011. Last inspected June 29, 2017.
Most cited issue areas
- Design input - documentation1 inspection
- DHR content1 inspection
- Justification for not reporting1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| June 29, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1018230 |
| September 19, 2013 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 851820 |
| June 9, 2011 | VAI | Medical Devices & Rad Health · Compliance: Devices | 734470 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Horiba ABX SAS
FEI Number
3000148879
Address
Parc Euromedecine, Rue Du Caducee, BP 7290, Montpellier, France
Country
France
ID: 4e7b68b7-a504-4a2d-9bf5-e13e0f3b8dde