FDA Inspection 1011333 - NuVasive, Inc - May 04, 2017

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Record Details

This FDA Inspection record concerns NuVasive, Inc, with an inspection on May 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: NuVasive, Inc
Inspection Date: May 4, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 91172305-b18d-4326-9659-64ab1ce0555b

Violation Codes3

21 CFR 806.20(b)(4)21 CFR 820.100(a)21 CFR 820.90(a)

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