FDA Inspection 986138 - KBL GmbH - September 02, 2016

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Record Details

This FDA Inspection record concerns KBL GmbH, with an inspection on September 2, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: KBL GmbH
Inspection Date: September 2, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ac2cd409-5e47-4954-9def-9175cfbe3bea