# Horiba Instruments Incorporated – FDA Inspection, Jan 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/horiba-instruments-incorporated/8f3472c7-9654-4f58-a779-a81d54f4abfa
Source feed: FDA_Inspections

> FDA inspection 627000 of Horiba Instruments Incorporated, January 15, 2010. Classification: Official Action Indicated (OAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 627000
- Company Name: Horiba Instruments Incorporated
- Inspection Date: 2010-01-15
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1031100 - 2017-10-31
- [FDA Inspection 931697 - 2015-06-30](https://www.keypedia.com/records/fda_inspections/horiba-instruments-incorporated/326b6a5b-2c6e-4b9a-ad42-46269ac30657)
- FDA Inspection 815527 - 2013-01-24
- FDA Inspection 782820 - 2012-03-09
- FDA Inspection 706493 - 2011-01-28

Company: https://www.keypedia.com/companies/horiba-instruments-incorporated/9012106e-e2bd-45d1-9ae9-3cfbd55e5b8c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7