FDA Inspection
Agilent Technologies, Inc.Agilent Technologies, Inc. – FDA Inspection, Feb 17, 2017
Record Details
This FDA Inspection record concerns Agilent Technologies, Inc., with an inspection on February 17, 2017, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Agilent Technologies, Inc.
- Inspection Date
- February 17, 2017
- Product Type
- Medical Devices & Rad Health
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ID · eca53227-26c7-4912-9d4e-fcaaa5f50367
Inspection Facts
- Inspection number
- 1007312
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 806.10(a)(2)Report of violation of the Act (see 803.52(e)(9))
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Other FDA inspections of Agilent Technologies, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 6, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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