# NuTech Spine, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/nutech-spine-inc/7864b0cd-7cf7-490b-b55a-82d524ac8c7e

> Inspection records and compliance data for NuTech Spine, Inc. in Birmingham, Alabama. Access full analysis and detailed observations.

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## Details

- Name: NuTech Spine, Inc.
- FEI Number: 3009169996
- City: Birmingham
- State: Alabama
- Country Name: United States
- Address Line 1: 2231 20th Ave S Ste 424
- Zip Code: 35223

## Related Documents

- [FDA Inspection 1155920 - NuTech Spine, Inc. - 2021-10-27](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/352cb63b-d22e-491a-adfa-7d1e3bd1713e) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2021
- [FDA Inspection 1155920 - NuTech Spine, Inc. - 2021-10-27](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/64b18db3-7c4d-4e96-9e54-c92e372d91b6) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2021
- [FDA Inspection 1094097 - NuTech Spine, Inc. - 2019-06-20](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/95477789-df9a-42ca-9226-3a7b1e415c8a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2019
- [FDA Inspection 1094097 - NuTech Spine, Inc. - 2019-06-20](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/345178b9-16f1-48ad-80f1-5ad5982dfff5) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2019
- [FDA Inspection 1056306 - NuTech Spine, Inc. - 2018-04-25](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/374d5282-1426-4dab-954e-b29b7b176a26) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2018
- [FDA Inspection 982009 - NuTech Spine, Inc. - 2016-07-13](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/57a5f46e-679f-4dbc-baef-59e336feaeee) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2016
- [FDA Inspection 884316 - NuTech Spine, Inc. - 2014-06-18](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/73e50228-f7dc-4760-a598-968c697bfb31) — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2014
- [FDA Inspection 833696 - NuTech Spine, Inc. - 2013-04-30](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/8321cbd6-dca5-47c7-8d21-3c8fe15cac94) — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2013
- [FDA Inspection 720781 - NuTech Spine, Inc. - 2011-04-07](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/9652d5bf-e285-42fe-86fb-be3fe8d6ef0e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 7, 2011
- [FDA Inspection 720781 - NuTech Spine, Inc. - 2011-04-07](https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/bf9cb23c-6c9c-49c9-b3a1-fc0f952f522c) — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2011

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