FDA Inspection 1031399 — Vectracor Inc

Vectracor Inc — FEI 1000520092

The FDA completed an inspection of Vectracor Inc on Oct 24, 2017 in Maple Grove, MN. 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
Oct 24, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)