# FDA Inspection 1074860 - BIALEX - December 17, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/bialex/32f71df9-a372-479a-bbd0-aeae3e39ba0f
Source feed: FDA_Inspections

> FDA Inspection 1074860 for BIALEX on December 17, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1074860
- Company Name: BIALEX
- Inspection Date: 2018-12-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1074860 - 2018-12-17](https://www.globalkeysolutions.net/records/fda_inspections/bialex/999836c5-7f4a-44ea-a9e2-1d6e835c2585)

Company: https://www.globalkeysolutions.net/companies/bialex/ed0799d0-1c94-45ff-8003-ff9c331cb04d

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