FDA Inspection 982009 — NuTech Spine, Inc.
The FDA completed an inspection of NuTech Spine, Inc. on July 13, 2016 in Birmingham, AL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 13, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Birmingham, AL (United States)