# Horiba Instruments Incorporated – FDA Inspection, May 16, 2013

Source: https://www.keypedia.com/records/fda_inspections/horiba-instruments-incorporated/82a8add5-c28e-4e20-ab14-0b9fc2b8f7e8
Source feed: FDA_Inspections

> FDA inspection 835525 of Horiba Instruments Incorporated, May 16, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 835525
- Company Name: Horiba Instruments Incorporated
- Inspection Date: 2013-05-16
- 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: 3

## Related Documents

- [FDA Inspection 771894 - 2012-03-01](https://www.keypedia.com/records/fda_inspections/horiba-instruments-incorporated/f9edfe0d-acaa-4341-9c16-a8551b0c563d)
- FDA Inspection 712341 - 2011-02-07
- FDA Inspection 671861 - 2010-07-13
- FDA Inspection 598173 - 2009-07-16

Company: https://www.keypedia.com/companies/horiba-instruments-incorporated/5821690b-d857-4726-ba06-f67cfd40afb0

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