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

Source: https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/9852a64e-b576-45f3-9b44-d56e524a3d2f
Source feed: FDA_Inspections

> FDA Inspection 1011333 for NuVasive, Inc on May 04, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1011333
- Company Name: NuVasive, Inc
- Inspection Date: 2017-05-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/nuvasive-inc/7d31c043-5e73-4ebf-b4c3-d1dcfa8306a4

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7