FDA Inspection
Horiba Instruments IncorporatedHoriba Instruments Incorporated – FDA Inspection, Mar 1, 2012
Record Details
This FDA Inspection record concerns Horiba Instruments Incorporated, with an inspection on March 1, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 1, 2012
- Product Type
- Devices
View Company Profile
ID · f9edfe0d-acaa-4341-9c16-a8551b0c563d
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 771894
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Horiba Instruments Incorporated
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 7, 2011 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| July 13, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 16, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Horiba Instruments Incorporated
- FDA Inspection 835525 - 2013-05-16
- FDA Inspection 712341 - 2011-02-07
- FDA Inspection 671861 - 2010-07-13
- FDA Inspection 598173 - 2009-07-16
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