FDA Inspection
Agilent Technologies, IncAgilent Technologies, Inc – FDA Inspection, Apr 14, 2009
Record Details
This FDA Inspection record concerns Agilent Technologies, Inc, with an inspection on April 14, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Agilent Technologies, Inc
- Inspection Date
- April 14, 2009
- Product Type
- Devices
View Company Profile
ID · 7e52141d-0f7b-4930-ae52-036c78f1c634
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 583585
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
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Other FDA inspections of Agilent Technologies, Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 30, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 14, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 15, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Agilent Technologies, Inc
- FDA Inspection 1202667 - 2023-03-30
- FDA Inspection 1046738 - 2018-03-14
- FDA Inspection 798314 - 2012-08-15
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