# FDA Inspection 969944 - Inovo, Inc - March 11, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/inovo-inc/575030d2-2ba5-427a-bc94-ab2e10b94a61
Source feed: FDA_Inspections

> FDA Inspection 969944 for Inovo, Inc on March 11, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969944
- Company Name: Inovo, Inc
- Inspection Date: 2016-03-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 969944 - 2016-03-11](https://www.globalkeysolutions.net/records/fda_inspections/inovo-inc/69fa8448-fee7-4518-8054-a0615ae35de2)
- [FDA Inspection 905359 - 2014-11-19](https://www.globalkeysolutions.net/records/fda_inspections/inovo-inc/c51af29a-2145-4549-9776-fb6180d4e315)
- [FDA Inspection 905359 - 2014-11-19](https://www.globalkeysolutions.net/records/fda_inspections/inovo-inc/25ec10ec-0ac2-4d30-bf33-4c2899e89c80)

Company: https://www.globalkeysolutions.net/companies/inovo-inc/736dbf08-9bba-45d7-8d10-36778a7c9092

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