FDA Inspection 1002820 - Fresenius Kabi USA, LLC - February 01, 2017

FDA Inspection 1002820 for Fresenius Kabi USA, LLC on February 01, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1002820 for Fresenius Kabi USA, LLC on February 01, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Fresenius Kabi USA, LLC

Inspection Date

February 1, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 252f9abd-eb39-4e89-a14e-68bb888a36c1

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