FDA Inspection 1216357 - Fresenius Kabi USA, LLC - August 30, 2023

FDA Inspection 1216357 for Fresenius Kabi USA, LLC on August 30, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1216357 for Fresenius Kabi USA, LLC on August 30, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Fresenius Kabi USA, LLC

Inspection Date

August 30, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 6b172d0c-ba88-4cda-9500-e353ae9c96c7

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