# FDA Inspection 1037116 - Tobii Dynavox Llc - December 15, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/tobii-dynavox-llc/74670172-233f-4cd5-9296-3b52a842a69a
Source feed: FDA_Inspections

> FDA Inspection 1037116 for Tobii Dynavox Llc on December 15, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037116
- Company Name: Tobii Dynavox Llc
- Inspection Date: 2017-12-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1037116 - 2017-12-15](https://www.globalkeysolutions.net/records/fda_inspections/tobii-dynavox-llc/2e8c0820-3354-4055-9df4-68b16571f953)

Company: https://www.globalkeysolutions.net/companies/tobii-dynavox-llc/951517c6-2f9d-4f26-986f-7dded5e2d3d1

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