# RSB Spine LLC, Cleveland, OH – FDA Inspections

Source: https://www.keypedia.com/companies/rsb-spine-llc/153342df-4d1e-4eca-b8ab-e9b5a39516c5

> Inspection records and compliance data for RSB Spine LLC in Cleveland, Ohio. 6 FDA inspections on record, 1 Form 483, last inspected July 28, 2025.

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## Details

- Name: RSB Spine LLC
- FEI Number: 3003597504
- Address Line 1: 2530 Superior Ave E Ste 703
- City: Cleveland
- State: Ohio
- Zip Code: 44114
- Country Name: United States
- Address: 2530 Superior Ave E Ste 703, Cleveland, Ohio 44114, United States
- Country: United States

## Related Documents

- FDA Inspection 1277043 - RSB Spine LLC - 2025-07-28 — source: FDA, date: July 28, 2025
- FDA Inspection 1277043 - RSB Spine LLC - 2025-07-28 — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2025
- [FDA Inspection 1035625 - RSB Spine LLC - 2017-12-21](https://www.keypedia.com/records/fda_inspections/rsb-spine-llc/ecdbba74-c0e8-486d-a38b-af56f9691b43) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2017
- FDA Inspection 1035625 - RSB Spine LLC - 2017-12-21 — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2017
- FDA Inspection 904052 - RSB Spine LLC - 2014-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2014
- FDA Inspection 904052 - RSB Spine LLC - 2014-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2014
- FDA Inspection 904052 - RSB Spine LLC - 2014-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2014
- FDA Inspection 842841 - RSB Spine LLC - 2013-08-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 6, 2013
- [FDA Inspection 842841 - RSB Spine LLC - 2013-08-06](https://www.keypedia.com/records/fda_inspections/rsb-spine-llc/d0cc626b-e471-4bb1-987a-5e721f81fa89) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 6, 2013
- FDA Inspection 756940 - RSB Spine LLC - 2011-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2011

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