FDA Inspection 1019824 - Fresenius Kabi USA LLC - July 20, 2017

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Record Details

This FDA Inspection record concerns Fresenius Kabi USA LLC, with an inspection on July 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Fresenius Kabi USA LLC
Inspection Date: July 20, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d2c8fc67-5e12-4f94-80ad-de6d402f6ac3