FDA Inspection
Agilent Technologies, Inc.Agilent Technologies, Inc. – FDA Inspection, Oct 1, 2012
Record Details
This FDA Inspection record concerns Agilent Technologies, Inc., with an inspection on October 1, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Agilent Technologies, Inc.
- Inspection Date
- October 1, 2012
- Product Type
- Devices
View Company Profile
ID · 267e6f42-57d1-42b6-8fc7-6a13b5bad15b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 801694
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Agilent Technologies, Inc.
9| Date | Classification | Office | Project area |
|---|---|---|---|
| July 17, 2025 | VAI | Los Angeles District Office | Product Evaluation: Medical Devices |
| September 29, 2021 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| December 6, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 25, 2018 | Not classified | Los Angeles District Office | |
| October 27, 2017 | Not classified | Los Angeles District Office |
Other documents for Agilent Technologies, Inc.
- FDA Inspection 1275852 - 2025-07-17
- FDA Inspection 1155499 - 2021-09-29
- FDA Inspection 1113860 - 2019-12-06
- FDA Inspection 1109059 - 2018-10-25
- FDA Inspection 1045809 - 2017-10-27
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