# Unified Spine, Llc - Inspection Records

Source: https://www.keypedia.com/companies/unified-spine-llc/8486d3fb-026d-4161-9a31-a1e7a0ffd074

> Inspection records and compliance data for Unified Spine, Llc in Westerville, Ohio. Access full analysis and detailed observations.

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## Details

- Name: Unified Spine, Llc
- FEI Number: 3006215390
- City: Westerville
- State: Ohio
- Country Name: United States
- Address Line 1: 6295 Maxtown Rd Ste 500
- Zip Code: 43082

## Related Documents

- [483 - Unified Spine, Llc - 2024-03-01](https://www.keypedia.com/records/483/unified-spine-llc/87960cba-cf7f-4568-afa2-f6fb24bb2f43) — source: FDA, date: March 1, 2024
- [FDA Inspection 1233724 - Unified Spine, Llc - 2024-03-01](https://www.keypedia.com/records/fda_inspections/unified-spine-llc/c81596e8-5137-4886-93ee-2e06b3bc84ed) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 1, 2024
- [FDA Inspection 1114511 - Unified Spine, Llc - 2019-12-04](https://www.keypedia.com/records/fda_inspections/unified-spine-llc/ae196b7e-3dd0-4c7c-ad4d-704ed7e02a0c) — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2019
- [FDA Inspection 1020853 - Unified Spine, Llc - 2017-07-06](https://www.keypedia.com/records/fda_inspections/unified-spine-llc/dbdd36e9-081f-4dbe-a67e-dc91badfd2f4) — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2017
- [FDA Inspection 983542 - Unified Spine, Llc - 2016-08-23](https://www.keypedia.com/records/fda_inspections/unified-spine-llc/b36aa2a0-8be2-4d04-aabc-d87075eb0b8e) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2016
- [FDA Inspection 983542 - Unified Spine, Llc - 2016-08-23](https://www.keypedia.com/records/fda_inspections/unified-spine-llc/e4e4a7ee-2b05-4181-a230-ec1a1e74e3b2) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2016
- [FDA Inspection 754612 - Unified Spine, Llc - 2011-11-18](https://www.keypedia.com/records/fda_inspections/unified-spine-llc/ea943dc2-6a25-4e77-ab06-251eb16789a9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2011

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