FDA Inspection 1026620 - Fresenius Kabi USA, LLC - August 18, 2017

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Record Details

This FDA Inspection record concerns Fresenius Kabi USA, LLC, with an inspection on August 18, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Fresenius Kabi USA, LLC
Inspection Date: August 18, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c0154c8a-66e0-490c-b1d5-2d7fd7926336