# FDA Inspection 1079240 - Cadence Device, Inc. - February 14, 2019

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

> FDA Inspection 1079240 for Cadence Device, Inc. on February 14, 2019. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1079240 - 2019-02-14](https://www.globalkeysolutions.net/records/fda_inspections/cadence-device-inc/34607f4b-00b5-41a4-b563-2f4f264d6d28)

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

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