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

FDA Inspection 1216357 for Fresenius Kabi USA, LLC on August 30, 2023. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1216357 for Fresenius Kabi USA, LLC on August 30, 2023. Classification: No Action Indicated (NAI).

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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: 7f0cd17c-920d-421e-8b7c-c5256d920e67

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