FDA Inspection 885395 — Life Spine, Inc.
The FDA completed an inspection of Life Spine, Inc. on Jun 30, 2014 in Huntley, 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
- Jun 30, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Huntley, IL (United States)