# Agilent Technologies, Inc – FDA Inspection, Apr 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/agilent-technologies-inc/7e52141d-0f7b-4930-ae52-036c78f1c634
Source feed: FDA_Inspections

> FDA inspection 583585 of Agilent Technologies, Inc, April 14, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 583585
- Company Name: Agilent Technologies, Inc
- Inspection Date: 2009-04-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1202667 - 2023-03-30
- FDA Inspection 1046738 - 2018-03-14
- FDA Inspection 798314 - 2012-08-15

Company: https://www.keypedia.com/companies/agilent-technologies-inc/7b262153-4855-46ed-b3ab-2882f698e0ed

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