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FDA Inspection
•Cadex Electronics, Inc.•January 9, 2026

Cadex Electronics, Inc. – FDA Inspection, Jan 9, 2026

Record Details

This FDA Inspection record concerns Cadex Electronics, Inc., with an inspection on January 9, 2026, issued by the Office of Inspections and Investigations, covering medical devices & rad health.

Company
Cadex Electronics, Inc.
Inspection Date
January 9, 2026
Product Type
Medical Devices & Rad Health
Office
Office of Inspections and Investigations
Person
  • Thai T. Duong (Issuing Officer)
View Company Profile

ID · ff05a129-2baa-48cf-b251-62d33296a3a7

Inspection Facts

Inspection number
1298110
FDA center
Medical Devices & Rad Health
Project area
Compliance: Medical Devices
Outcome
Form 483 issued, view the record

FDA Citations

4
  1. 21 CFR 820.120Lack of or inadequate procedures for labeling
  2. 21 CFR 820.198(a)Lack of or inadequate complaint procedures
  3. 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
  4. 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cadex Electronics, Inc.

3
DateClassificationOfficeProject area
February 9, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 24, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
June 8, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Cadex Electronics, Inc.
  • FDA Inspection 1199832 - 2023-02-09
  • FDA Inspection 1060263 - 2018-05-24
  • FDA Inspection 731948 - 2011-06-08

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