# NuTech Spine, Inc., Birmingham, AL – FDA Inspections

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. 7 FDA inspections on record, 1 Form 483, last inspected October 27, 2021.

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## Details

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

## Related Documents

- FDA Inspection 1155920 - NuTech Spine, Inc. - 2021-10-27 — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2021
- FDA Inspection 1155920 - NuTech Spine, Inc. - 2021-10-27 — 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 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2019
- FDA Inspection 1056306 - NuTech Spine, Inc. - 2018-04-25 — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2018
- FDA Inspection 982009 - NuTech Spine, Inc. - 2016-07-13 — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2016
- FDA Inspection 884316 - NuTech Spine, Inc. - 2014-06-18 — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2014
- FDA Inspection 833696 - NuTech Spine, Inc. - 2013-04-30 — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2013
- FDA Inspection 720781 - NuTech Spine, Inc. - 2011-04-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 7, 2011
- FDA Inspection 720781 - NuTech Spine, Inc. - 2011-04-07 — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2011

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