# FDA Inspection 738375 - Oxus, Inc. - August 01, 2011

Source: https://www.keypedia.com/records/fda_inspections/oxus-inc/eab08887-ae35-4dc1-9d4d-554dee0dd0c2
Source feed: FDA_Inspections

> FDA Inspection 738375 for Oxus, Inc. on August 01, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 738375
- Company Name: Oxus, Inc.
- Inspection Date: 2011-08-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1106131 - 2019-10-10](https://www.keypedia.com/records/fda_inspections/oxus-inc/011e6be9-d2fc-4a6a-be83-2355effec7d5)
- [FDA Inspection 1106131 - 2019-10-10](https://www.keypedia.com/records/fda_inspections/oxus-inc/0ae10be7-970a-427a-85e6-a80736ddbfed)
- [FDA Inspection 956232 - 2016-01-19](https://www.keypedia.com/records/fda_inspections/oxus-inc/38ca1d3a-6f3b-4aec-8a53-ad83f0bfa489)
- [FDA Inspection 848933 - 2013-09-20](https://www.keypedia.com/records/fda_inspections/oxus-inc/9b79b0ad-d133-4c69-8200-76e3b6b27a60)
- [FDA Inspection 848933 - 2013-09-20](https://www.keypedia.com/records/fda_inspections/oxus-inc/c4b45f6e-d964-48c5-9f99-a7849c00149f)

Company: https://www.keypedia.com/companies/oxus-inc/3fe719af-2bb0-4264-8024-b751243ae8f3

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