FDA Inspection 985974 — SpineCraft, LLC.
The FDA completed an inspection of SpineCraft, LLC. on Aug 18, 2016 in Westmont, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 18, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Westmont, IL (United States)