# FDA Inspection 1010582 - Agilent Technologies, Inc. - January 13, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/agilent-technologies-inc/de2d3061-e074-4e07-9f56-6b68d602bd90
Source feed: FDA_Inspections

> FDA Inspection 1010582 for Agilent Technologies, Inc. on January 13, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010582
- Company Name: Agilent Technologies, Inc.
- Inspection Date: 2017-01-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/agilent-technologies-inc/480d273c-0e5e-44b6-b766-a13ec00b422c

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