FDA Inspection
Agilent Technologies, Inc.Agilent Technologies, Inc. – FDA Inspection, Oct 27, 2017
Record Details
This FDA Inspection record concerns Agilent Technologies, Inc., with an inspection on October 27, 2017, issued by the Los Angeles District Office, covering medical devices & rad health.
- Company
- Agilent Technologies, Inc.
- Inspection Date
- October 27, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 2812241b-09fb-442f-b2dc-99b34af39474
Inspection Facts
- Inspection number
- 1045809
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 | |
| January 13, 2017 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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 1010582 - 2017-01-13
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