# FDA Inspection 963722 - Vexos - March 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/vexos/c4523fee-0147-4033-84c2-c5abb4acc408
Source feed: FDA_Inspections

> FDA Inspection 963722 for Vexos on March 17, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 963722
- Company Name: Vexos
- Inspection Date: 2016-03-17
- 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 963722 - 2016-03-17](https://www.keypedia.com/records/fda_inspections/vexos/bc81680c-284e-4f35-a034-ff39779830aa)

Company: https://www.keypedia.com/companies/vexos/65e9deda-1a1c-4bf5-b3b6-1dfa1492b658

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