FDA Inspection 777309 — SpineCraft, LLC.
The FDA completed an inspection of SpineCraft, LLC. on Apr 12, 2012 in Westmont, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 12, 2012
- Fiscal Year
- 2012
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Westmont, IL (United States)