# FDA Inspection 1016120 - XIROS Ltd - June 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/xiros-ltd/42eeeda1-2e44-4639-8fda-67e6a26b9db2
Source feed: FDA_Inspections

> FDA Inspection 1016120 for XIROS Ltd on June 29, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016120
- Company Name: XIROS Ltd
- Inspection Date: 2017-06-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1016120 - 2017-06-29](https://www.keypedia.com/records/fda_inspections/xiros-ltd/b86c3022-afb2-4dca-9a3e-898c4f7582d0)
- [FDA Inspection 875520 - 2014-03-20](https://www.keypedia.com/records/fda_inspections/xiros-ltd/befb65ad-3745-4a95-8ed0-7ea4c84b4d88)

Company: https://www.keypedia.com/companies/xiros-ltd/cf685830-d8ab-470e-8e74-6fb22c85b6ef

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