# FDA Inspection 890552 - UE LifeSciences Inc. - August 07, 2014

Source: https://www.keypedia.com/records/fda_inspections/ue-lifesciences-inc/1bfc7f83-1500-4c71-8616-ef9a82e08bb5
Source feed: FDA_Inspections

> FDA Inspection 890552 for UE LifeSciences Inc. on August 07, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 890552
- Company Name: UE LifeSciences Inc.
- Inspection Date: 2014-08-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 948445 - 2015-10-26](https://www.keypedia.com/records/fda_inspections/ue-lifesciences-inc/7f5c3b71-8cca-4644-ac3d-d69542fc15bd)
- [FDA Inspection 890552 - 2014-08-07](https://www.keypedia.com/records/fda_inspections/ue-lifesciences-inc/01f8ba6c-55a0-4a40-a99c-e6ced91cc635)

Company: https://www.keypedia.com/companies/ue-lifesciences-inc/71a01cae-5104-420f-aa93-e2d0509b95dd

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