FDA Inspection 946577 - Neurolumen LLC - October 22, 2015

FDA Inspection 946577 for Neurolumen LLC on October 22, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 946577 for Neurolumen LLC on October 22, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Neurolumen LLC

Inspection Date

October 22, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 201e0bee-a2a3-4725-a270-3f480ce50922

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