# RSB Spine LLC – FDA Inspection, Dec 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/rsb-spine-llc/ecdbba74-c0e8-486d-a38b-af56f9691b43
Source feed: FDA_Inspections

> FDA inspection 1035625 of RSB Spine LLC, December 21, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035625
- Company Name: RSB Spine LLC
- Inspection Date: 2017-12-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1277043 - 2025-07-28
- FDA Inspection 904052 - 2014-12-04
- [FDA Inspection 842841 - 2013-08-06](https://www.keypedia.com/records/fda_inspections/rsb-spine-llc/d0cc626b-e471-4bb1-987a-5e721f81fa89)
- FDA Inspection 756940 - 2011-12-13
- FDA Inspection 663207 - 2010-05-21

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
