# FDA Inspection 1101121 - NuVasive, Inc - July 29, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/d411574b-1e31-4b36-a26d-8ca6ec01425b
Source feed: FDA_Inspections

> FDA Inspection 1101121 for NuVasive, Inc on July 29, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101121
- Company Name: NuVasive, Inc
- Inspection Date: 2019-07-29
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/nuvasive-inc/7d31c043-5e73-4ebf-b4c3-d1dcfa8306a4

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