# FDA Inspection 598173 - Horiba Instruments Incorporated - July 16, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/horiba-instruments-incorporated/2c34c63b-f51e-4d1b-8d57-18904b197fcc
Source feed: FDA_Inspections

> FDA Inspection 598173 for Horiba Instruments Incorporated on July 16, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598173
- Company Name: Horiba Instruments Incorporated
- Inspection Date: 2009-07-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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