FDA Inspection 958734 — Neochord Inc

Neochord Inc — FEI 3009758645

The FDA completed an inspection of Neochord Inc on Dec 21, 2015 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
Dec 21, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)