# SpineCraft, LLC., Westmont, IL – FDA Inspections

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

> Inspection records and compliance data for SpineCraft, LLC. in Westmont, Illinois. 5 FDA inspections on record, last inspected March 22, 2024.

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## Details

- Name: SpineCraft, LLC.
- FEI Number: 3004717358
- Address Line 1: 777 Oakmont Ln Ste 200
- City: Westmont
- State: Illinois
- Zip Code: 60559
- Country Name: United States
- Address: 777 Oakmont Ln Ste 200, Westmont, Illinois 60559, United States
- Country: United States

## Related Documents

- [FDA Inspection 1233747 - SpineCraft, LLC. - 2024-03-22](https://www.keypedia.com/records/fda_inspections/spinecraft-llc/9435c7d6-bd9c-43aa-81e4-7314d53bb8ca) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 22, 2024
- FDA Inspection 1074762 - SpineCraft, LLC. - 2018-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- FDA Inspection 1074762 - SpineCraft, LLC. - 2018-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- FDA Inspection 1073334 - SpineCraft, LLC. - 2018-11-14 — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2018
- FDA Inspection 985974 - SpineCraft, LLC. - 2016-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2016
- FDA Inspection 985974 - SpineCraft, LLC. - 2016-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2016
- FDA Inspection 985974 - SpineCraft, LLC. - 2016-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2016
- FDA Inspection 777309 - SpineCraft, LLC. - 2012-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2012
- FDA Inspection 777309 - SpineCraft, LLC. - 2012-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2012
- FDA Inspection 777309 - SpineCraft, LLC. - 2012-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2012

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