# FDA Inspection 1040485 - Cadence Inc - December 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/cadence-inc/2f7fcf0e-12f0-4d7c-9b1d-02c993f0c37b
Source feed: FDA_Inspections

> FDA Inspection 1040485 for Cadence Inc on December 14, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040485
- Company Name: Cadence Inc
- Inspection Date: 2017-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1040485 - 2017-12-14](https://www.keypedia.com/records/fda_inspections/cadence-inc/bd24e3a8-7778-4793-8f91-73569be9163d)

Company: https://www.keypedia.com/companies/cadence-inc/de5433cb-a742-48b6-8382-a9d1e416360b

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