# NuVasive, Inc - Inspection Records

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

> Inspection records and compliance data for NuVasive, Inc in Memphis, Tennessee. Access full analysis and detailed observations.

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## Details

- Name: NuVasive, Inc
- FEI Number: 3005949151
- City: Memphis
- State: Tennessee
- Country Name: United States
- Address Line 1: 4670 E Shelby Dr
- Zip Code: 38118

## Related Documents

- [FDA Inspection 1229391 - NuVasive, Inc - 2024-01-30](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/fc799ae2-4536-4cf9-b8e2-590ff7a24504) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2024
- [FDA Inspection 1120583 - NuVasive, Inc - 2020-02-07](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/4607f8ea-d280-4e4d-900b-db8c0ff0c45b) — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2020
- [FDA Inspection 1101121 - NuVasive, Inc - 2019-07-29](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/d411574b-1e31-4b36-a26d-8ca6ec01425b) — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2019
- [483 - NuVasive, Inc - 2017-05-04](https://www.globalkeysolutions.net/records/483/nuvasive-inc/a5b1b8c4-2678-4e2b-898b-29e4f230f731) — source: FDA, date: May 4, 2017
- [FDA Inspection 1011333 - NuVasive, Inc - 2017-05-04](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/91172305-b18d-4326-9659-64ab1ce0555b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2017
- [FDA Inspection 1011333 - NuVasive, Inc - 2017-05-04](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/9852a64e-b576-45f3-9b44-d56e524a3d2f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 4, 2017
- [FDA Inspection 1002060 - NuVasive, Inc - 2017-01-19](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/05ca664b-5f64-4154-bcc4-fbc9f03d9392) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2017
- [FDA Inspection 885327 - NuVasive, Inc - 2014-06-26](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/df02aa2b-4fef-445a-ba3e-a58c6ba59985) — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2014
- [483 - NuVasive, Inc - 2014-03-14](https://www.globalkeysolutions.net/records/483/nuvasive-inc/ecd002f0-0558-4d40-9819-09299fb00a1f) — source: FDA, date: March 14, 2014
- [FDA Inspection 869876 - NuVasive, Inc - 2014-03-14](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/410226b4-8afa-41c7-af0f-4424a62f0555) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2014
- [FDA Inspection 795255 - NuVasive, Inc - 2012-08-08](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/fb22f0a9-2450-463b-95b1-f117744400dc) — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2012
- [FDA Inspection 788944 - NuVasive, Inc - 2012-06-29](https://www.globalkeysolutions.net/records/fda_inspections/nuvasive-inc/9a3f63b9-0fb9-4c35-9c20-d40301fb69f4) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2012

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## Related Officers

- [Investigator/Consumer Safety Officer](https://www.globalkeysolutions.net/people/francis-a-guidry/fd6d2a17-7f94-4f7c-8284-ad1f07d703e9)
- [issuing_officer](https://www.globalkeysolutions.net/people/bonnie-b-conley/9d0d68d2-f40f-455d-a33e-3d5d1e97f295)