# NuVasive Inc – FDA Inspection, Dec 2, 2008

Source: https://www.keypedia.com/records/fda_inspections/nuvasive-inc/d0196b3b-5e61-43e9-837a-89f12a2dec54
Source feed: FDA_Inspections

> FDA inspection 548750 of NuVasive Inc, December 02, 2008. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 548750
- Company Name: NuVasive Inc
- Inspection Date: 2008-12-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1011810 - 2017-05-26](https://www.keypedia.com/records/fda_inspections/nuvasive-inc/9ee078f9-f3d5-47e6-852d-541e170cfb11)
- FDA Inspection 904804 - 2014-11-19
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- [FDA Inspection 805149 - 2012-11-02](https://www.keypedia.com/records/fda_inspections/nuvasive-inc/d1323377-47a0-4483-bef6-31688ebd0805)
- FDA Inspection 768996 - 2012-02-10

Company: https://www.keypedia.com/companies/nuvasive-inc/b60df9db-c2cf-4c29-abf9-4ae91cbe363a

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