FDA Inspection 1062329 - Vygon GmbH & Co. KG - August 16, 2018

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Record Details

This FDA Inspection record concerns Vygon GmbH & Co. KG, with an inspection on August 16, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vygon GmbH & Co. KG
Inspection Date: August 16, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5706339a-0cbb-47a8-9d3a-5f6dcea68c17