# Agilent Technologies, Inc. – FDA Inspection, Jul 6, 2015

Source: https://www.keypedia.com/records/fda_inspections/agilent-technologies-inc/ee543d16-337c-4f44-bec4-3c97daba44e7
Source feed: FDA_Inspections

> FDA inspection 936087 of Agilent Technologies, Inc., July 06, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 936087
- Company Name: Agilent Technologies, Inc.
- Inspection Date: 2015-07-06
- 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: 2

## Related Documents

- [FDA Inspection 1007312 - 2017-02-17](https://www.keypedia.com/records/fda_inspections/agilent-technologies-inc/eca53227-26c7-4912-9d4e-fcaaa5f50367)

Company: https://www.keypedia.com/companies/agilent-technologies-inc/923cc556-27ac-40a7-b96d-e813aa42743b

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