FDA Inspection
Agilent Technologies, Inc.Agilent Technologies, Inc. – FDA Inspection, Jul 6, 2015
Record Details
This FDA Inspection record concerns Agilent Technologies, Inc., with an inspection on July 6, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Agilent Technologies, Inc.
- Inspection Date
- July 6, 2015
- Product Type
- Devices
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ID · ee543d16-337c-4f44-bec4-3c97daba44e7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 936087
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.120Lack of or inadequate procedures for labeling
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Other FDA inspections of Agilent Technologies, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 17, 2017 | Not classified | San Francisco District Office | Compliance: Devices |
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