FDA Inspection 910131 — Monteris Medical Corp

Monteris Medical Corp — FEI 3009970070

The FDA completed an inspection of Monteris Medical Corp on Nov 14, 2014 in Minnetonka, 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
Nov 14, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)