# NuVasive, Inc – FDA Inspection, May 4, 2017

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

> FDA inspection 1011333 of NuVasive, Inc, May 04, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. Form 483 issued. 11 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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## Related Officers

- Issuing Officer

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