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

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