FDA Inspection 1058697 — Nuvectra Corporation

Nuvectra Corporation — FEI 3010309840

The FDA completed an inspection of Nuvectra Corporation on June 11, 2018 in Blaine, MN. 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
June 11, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Blaine, MN (United States)