FDA Inspection 809863 - Fresenius U.S.A. Manufacturing - December 27, 2012

FDA Inspection 809863 for Fresenius U.S.A. Manufacturing on December 27, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 809863 for Fresenius U.S.A. Manufacturing on December 27, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Fresenius U.S.A. Manufacturing

Inspection Date

December 27, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7fdd9f5-68c8-4d97-9aa5-65638e62f242

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