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

Source: https://www.keypedia.com/records/fda_inspections/nuvasive-inc/f9350ca0-e7cb-4e1e-9d60-e1439fa6ae13
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 616384
- Company Name: NuVasive, Inc
- Inspection Date: 2009-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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