# FDA Inspection 991304 - Nuvasive Inc - October 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/nuvasive-inc/9c94a3af-8aba-4df1-be55-a80ace98adce
Source feed: FDA_Inspections

> FDA Inspection 991304 for Nuvasive Inc on October 26, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991304
- Company Name: Nuvasive Inc
- Inspection Date: 2016-10-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 991304 - 2016-10-26](https://www.keypedia.com/records/fda_inspections/nuvasive-inc/c1758c68-3aea-40a5-bf07-cfed24ede39a)
- [FDA Inspection 892478 - 2014-08-27](https://www.keypedia.com/records/fda_inspections/nuvasive-inc/60904a88-265d-42b8-9fd1-7c4a5c103415)
- [FDA Inspection 892478 - 2014-08-27](https://www.keypedia.com/records/fda_inspections/nuvasive-inc/f9a6030a-7b16-4a6c-94e6-a8b19935e60b)

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