# FDA Inspection 966276 - De Novo Software - March 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/de-novo-software/73d7e64f-7c80-4400-a023-b16a95ed74ca
Source feed: FDA_Inspections

> FDA Inspection 966276 for De Novo Software on March 23, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 966276
- Company Name: De Novo Software
- Inspection Date: 2016-03-23
- 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 966276 - 2016-03-23](https://www.keypedia.com/records/fda_inspections/de-novo-software/9c34089e-33e4-4b8e-add1-6d57f13a8408)
- [FDA Inspection 886592 - 2014-07-09](https://www.keypedia.com/records/fda_inspections/de-novo-software/b9ab7a3e-c5f3-4469-b54f-55b5c964d3ab)

Company: https://www.keypedia.com/companies/de-novo-software/2e9ef2f1-c344-47b2-9ae2-cc7784362a1a

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