FDA Inspection 1012391 - LRE Medical GmbH - February 03, 2017

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Record Details

This FDA Inspection record concerns LRE Medical GmbH, with an inspection on February 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: LRE Medical GmbH
Inspection Date: February 3, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 376b49f0-d54c-4732-95bb-8583a71d9851