FDA Inspection
Cadence Device, Inc.Cadence Device, Inc. – FDA Inspection, Feb 14, 2019
Record Details
This FDA Inspection record concerns Cadence Device, Inc., with an inspection on February 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6103a0a7-d499-41f3-99e2-8ff5c22027a7
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1079240
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Cadence Device, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 7, 2026 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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