FDA Inspection 1014500 - Nuvasive PR, Inc. - May 31, 2017

FDA Inspection 1014500 for Nuvasive PR, Inc. on May 31, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1014500 for Nuvasive PR, Inc. on May 31, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Nuvasive PR, Inc.

Inspection Date

May 31, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8e1a604-16a8-455c-bb3e-b50d09c5f58b

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