# FDA Inspection 1113860 - Agilent Technologies, Inc. - December 06, 2019

Source: https://www.keypedia.com/records/fda_inspections/agilent-technologies-inc/e59e6b95-1002-401b-bf57-38939ecd6dfa
Source feed: FDA_Inspections

> FDA Inspection 1113860 for Agilent Technologies, Inc. on December 06, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1113860
- Company Name: Agilent Technologies, Inc.
- Inspection Date: 2019-12-06
- Classification: No Action Indicated (NAI)
- 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