# Cadence Device, Inc. – FDA Inspection, Feb 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/cadence-device-inc/6103a0a7-d499-41f3-99e2-8ff5c22027a7
Source feed: FDA_Inspections

> FDA inspection 1079240 of Cadence Device, Inc., February 14, 2019. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079240
- Company Name: Cadence Device, Inc.
- Inspection Date: 2019-02-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1316828 - 2026-05-07](https://www.keypedia.com/records/fda_inspections/cadence-device-inc/d7fdb1c4-0455-4c42-a377-d83b253fe437)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/katelyn-a-staub-zamperini/bb7f95a4-53c1-473c-856e-517312bdba30)

Company: https://www.keypedia.com/companies/cadence-device-inc/fa92e7c5-6998-4ccc-b12b-0a44a0a2d57e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7