# FDA Inspection 886592 - De Novo Software - July 09, 2014

Source: https://www.keypedia.com/records/fda_inspections/de-novo-software/b9ab7a3e-c5f3-4469-b54f-55b5c964d3ab
Source feed: FDA_Inspections

> FDA Inspection 886592 for De Novo Software on July 09, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 886592
- Company Name: De Novo Software
- Inspection Date: 2014-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 966276 - 2016-03-23](https://www.keypedia.com/records/fda_inspections/de-novo-software/73d7e64f-7c80-4400-a023-b16a95ed74ca)

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