FDA Inspection 675290 - Alive Inc. DBA Hako-Med - August 12, 2010

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Record Details

This FDA Inspection record concerns Alive Inc. DBA Hako-Med, with an inspection on August 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Alive Inc. DBA Hako-Med
Inspection Date: August 12, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 76a24f1e-15a7-4985-a5c9-8ae4888305d5