# FDA Inspection 1056265 - Biomedix Wai - June 08, 2018

Source: https://www.keypedia.com/records/fda_inspections/biomedix-wai/39e96508-58cd-4e5f-b152-ba8dc19d54c5
Source feed: FDA_Inspections

> FDA Inspection 1056265 for Biomedix Wai on June 08, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056265
- Company Name: Biomedix Wai
- Inspection Date: 2018-06-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/biomedix-wai/35aa0e7f-c8eb-40a8-9b5b-5b57fa435abf

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