# SpineCraft, LLC. – FDA Inspection, Mar 22, 2024

Source: https://www.keypedia.com/records/fda_inspections/spinecraft-llc/9435c7d6-bd9c-43aa-81e4-7314d53bb8ca
Source feed: FDA_Inspections

> FDA inspection 1233747 of SpineCraft, LLC., March 22, 2024. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1233747
- Company Name: SpineCraft, LLC.
- Inspection Date: 2024-03-22
- 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: 2

## Related Documents

- FDA Inspection 1074762 - 2018-12-13
- FDA Inspection 1073334 - 2018-11-14
- FDA Inspection 985974 - 2016-08-18
- FDA Inspection 777309 - 2012-04-12

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

Company: https://www.keypedia.com/companies/spinecraft-llc/1f8afee0-4555-47a4-93df-1b10a279b5bc

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