FDA Inspection 859558 - Neurolumen LLC - December 13, 2013

FDA Inspection 859558 for Neurolumen LLC on December 13, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 859558 for Neurolumen LLC on December 13, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Neurolumen LLC

Inspection Date

December 13, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd61281f-e1cd-405b-8068-f851862e10aa

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