FDA Inspection 1058912 — Nuvectra Corporation

Nuvectra Corporation — FEI 3011874692

The FDA completed an inspection of Nuvectra Corporation on Mar 26, 2018 in Plano, TX. 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
Mar 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Plano, TX (United States)