FDA Inspection 988687 - Ivoclar Vivadent Manufacturing GmbH - August 26, 2016

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Record Details

This FDA Inspection record concerns Ivoclar Vivadent Manufacturing GmbH, with an inspection on August 26, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Ivoclar Vivadent Manufacturing GmbH
Inspection Date: August 26, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 997cb0d9-44a6-440a-ab9a-adc4566a7203