FDA Inspection 850919 - Mizuho OSI - September 25, 2013

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Record Details

This FDA Inspection record concerns Mizuho OSI, with an inspection on September 25, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Mizuho OSI
Inspection Date: September 25, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6882dfc9-939a-4ae9-9364-6fa2926a6deb