FDA Inspection
Horiba Instruments IncorporatedHoriba Instruments Incorporated – FDA Inspection, Jun 30, 2015
Record Details
This FDA Inspection record concerns Horiba Instruments Incorporated, with an inspection on June 30, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 30, 2015
- Product Type
- Devices
View Company Profile
ID · 326b6a5b-2c6e-4b9a-ad42-46269ac30657
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 931697
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Horiba Instruments Incorporated
6| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 24, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 9, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 28, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 15, 2010 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Horiba Instruments Incorporated
- FDA Inspection 1031100 - 2017-10-31
- FDA Inspection 815527 - 2013-01-24
- FDA Inspection 782820 - 2012-03-09
- FDA Inspection 706493 - 2011-01-28
- FDA Inspection 627000 - 2010-01-15
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