# FDA Inspection 935001 - Amvex Corporation - June 18, 2015

Source: https://www.keypedia.com/records/fda_inspections/amvex-corporation/409504d5-abbf-4e5f-8bd0-b31d2c57cb98
Source feed: FDA_Inspections

> FDA Inspection 935001 for Amvex Corporation on June 18, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935001
- Company Name: Amvex Corporation
- Inspection Date: 2015-06-18
- 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/amvex-corporation/f228360d-e36d-427f-947f-cb0379094754

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