# FDA Inspection 946183 - Agilent Technologies, Inc. - October 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/agilent-technologies-inc/c0be36f7-cfbd-40fe-b937-82a1b04a5e71
Source feed: FDA_Inspections

> FDA Inspection 946183 for Agilent Technologies, Inc. on October 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 946183
- Company Name: Agilent Technologies, Inc.
- Inspection Date: 2015-10-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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