FDA Inspection 1094097 — NuTech Spine, Inc.

NuTech Spine, Inc. — FEI 3009169996

The FDA completed an inspection of NuTech Spine, Inc. on June 20, 2019 in Birmingham, AL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 20, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Birmingham, AL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures