FDA Inspection 884787 - Diasorin Deutschland GmbH - May 30, 2014

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Record Details

This FDA Inspection record concerns Diasorin Deutschland GmbH, with an inspection on May 30, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Diasorin Deutschland GmbH
Inspection Date: May 30, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6f4ecf51-aeb8-46e4-8448-c74a51f9f771

Violation Codes2

21 CFR 820.70(c)21 CFR 820.70(i)

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