# Agilent Technologies, Inc. – FDA Inspection, Oct 1, 2012

Source: https://www.keypedia.com/records/fda_inspections/agilent-technologies-inc/267e6f42-57d1-42b6-8fc7-6a13b5bad15b
Source feed: FDA_Inspections

> FDA inspection 801694 of Agilent Technologies, Inc., October 01, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 801694
- Company Name: Agilent Technologies, Inc.
- Inspection Date: 2012-10-01
- 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: 1

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

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