FDA Inspection 1003090 - Beckman Coulter GmbH - February 02, 2017

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Record Details

This FDA Inspection record concerns Beckman Coulter GmbH, with an inspection on February 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Beckman Coulter GmbH
Inspection Date: February 2, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1adc7700-f7e1-45e0-9c8a-929b44714950

Violation Codes2

21 CFR 820.80(e)21 CFR 820.90(a)

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