FDA Inspection
Cadex Electronics, Inc.Cadex Electronics, Inc. – FDA Inspection, Jun 8, 2011
Record Details
This FDA Inspection record concerns Cadex Electronics, Inc., with an inspection on June 8, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Cadex Electronics, Inc.
- Inspection Date
- June 8, 2011
- Product Type
- Devices
View Company Profile
ID · 9b0705b5-477a-4ee4-b650-189915e65705
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 731948
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.30(f)Design verification - output does not meet input requirement
- 21 CFR 820.30(e)Design review - Lack of or inadequate procedures
- 21 CFR 820.30(e)Design review - documentation
- 21 CFR 820.184DHR content
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cadex Electronics, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 9, 2026 | Not classified | Office of Inspections and Investigations | Compliance: Medical Devices |
| February 9, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 24, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cadex Electronics, Inc.
- FDA Inspection 1298110 - 2026-01-09
- FDA Inspection 1199832 - 2023-02-09
- FDA Inspection 1060263 - 2018-05-24
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