# FDA Inspection 925870 - BIOVISION - April 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/biovision/956821c5-29b1-47bc-85e2-ed9a383a41b1
Source feed: FDA_Inspections

> FDA Inspection 925870 for BIOVISION on April 30, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 925870
- Company Name: BIOVISION
- Inspection Date: 2015-04-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/biovision/af9c15ff-3554-45e0-b899-d8448a2275a7

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