# FDA 483 - NuVasive, Incorporated - December 21, 2020

Source: https://www.globalkeysolutions.net/records/483/nuvasive-incorporated/aaa48c6c-f44f-4226-b6ba-4703900c49f1

> FDA 483 for NuVasive, Incorporated on December 21, 2020. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: NuVasive, Incorporated
- Inspection Date: 2020-12-21
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
- Summary: This FDA Form 483 report for NuVasive, Incorporated indicates that no inspectional observations were noted during the inspection. The report suggests that the firm was found to be in compliance with regulatory requirements at the time of the inspection.

## Related Officers

- [Jennifer Houck](https://www.globalkeysolutions.net/people/jennifer-houck/3f3e4c8c-8b2b-46e9-a740-7ca3c31ea68b)

Company: https://www.globalkeysolutions.net/companies/nuvasive-incorporated/338ec3b6-5c4b-4d11-a7d0-d0065209070a

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd