FDA Inspection 832575 - Neurolign USA, Llc - May 17, 2013

FDA Inspection 832575 for Neurolign USA, Llc on May 17, 2013. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 832575 for Neurolign USA, Llc on May 17, 2013. Classification: Official Action Indicated (OAI).

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Record Information

Company

Neurolign USA, Llc

Inspection Date

May 17, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc8602b5-5b82-4332-9eac-83af2641eb03

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