FDA Inspection 1016857 — Nuvectra Corporation

Nuvectra Corporation — FEI 3010309840

The FDA completed an inspection of Nuvectra Corporation on April 12, 2017 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
April 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Blaine, MN (United States)

Additional Details

Postmarket Audit Inspections