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FDA Inspection
•Cadence Device, Inc.•May 7, 2026

Cadence Device, Inc. – FDA Inspection, May 7, 2026

Record Details

This FDA Inspection record concerns Cadence Device, Inc., with an inspection on May 7, 2026, issued by the Center for Devices and Radiological Health, covering medical devices & rad health.

Company
Cadence Device, Inc.
Inspection Date
May 7, 2026
Product Type
Medical Devices & Rad Health
Office
Center for Devices and Radiological Health
Person
  • Dennis R. Hock (Company Rep)
View Company Profile

ID · d7fdb1c4-0455-4c42-a377-d83b253fe437

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1316828
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Cadence Device, Inc.

1
DateClassificationOfficeProject area
February 14, 2019NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Cadence Device, Inc.
  • FDA Inspection 1079240 - 2019-02-14

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