FDA Inspection 926048 - Endoplus - May 19, 2015

FDA Inspection 926048 for Endoplus on May 19, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 926048 for Endoplus on May 19, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Endoplus

Inspection Date

May 19, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb5ddfe5-2517-4b86-b6b0-8dd5a69c66de

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