FDA Inspection 996791 - SPINEART SA - December 08, 2016

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Record Details

This FDA Inspection record concerns SPINEART SA, with an inspection on December 8, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: SPINEART SA
Inspection Date: December 8, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 32c3096a-23ae-412c-9970-527ba6b8f503