FDA Inspection 1113433 - Fresenius Kabi USA, LLC - November 25, 2019

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Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on November 25, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Fresenius Kabi USA, LLC
Inspection Date: November 25, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 48917e5b-329f-4aea-9f14-36d3855219c1