# Nuvasive Inc – FDA Inspection, Oct 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/nuvasive-inc/c1758c68-3aea-40a5-bf07-cfed24ede39a
Source feed: FDA_Inspections

> FDA inspection 991304 of Nuvasive Inc, October 26, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991304
- Company Name: Nuvasive Inc
- Inspection Date: 2016-10-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 892478 - 2014-08-27

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/nuvasive-inc/04222261-8266-4c81-ad5b-3b361bbfeb18

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