FDA Inspection 640523 - Fresenius Kabi USA, LLC - January 21, 2010

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Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on January 21, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Fresenius Kabi USA, LLC
Inspection Date: January 21, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d5e3d4e7-ffcf-4998-8061-9a56dc8540d8