# Horiba Instruments Incorporated – FDA Inspection, Apr 8, 2009

Source: https://www.keypedia.com/records/fda_inspections/horiba-instruments-incorporated/9cf76fa1-2ff3-4e99-bc0a-fe1e23077fdc
Source feed: FDA_Inspections

> FDA inspection 577506 of Horiba Instruments Incorporated, April 08, 2009. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 806 and 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 577506
- Company Name: Horiba Instruments Incorporated
- Inspection Date: 2009-04-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## 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