FDA Inspection 616384 - NuVasive, Inc - September 18, 2009

FDA Inspection 616384 for NuVasive, Inc on September 18, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 616384 for NuVasive, Inc on September 18, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

NuVasive, Inc

Inspection Date

September 18, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9350ca0-e7cb-4e1e-9d60-e1439fa6ae13

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