FDA Inspection 979231 - Abiomed Europe GmbH - June 23, 2016

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Record Details

This FDA Inspection record concerns Abiomed Europe GmbH, with an inspection on June 23, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Abiomed Europe GmbH
Inspection Date: June 23, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 680fc4e9-e70d-4591-a6b8-fb8104050d8d