FDA Inspection 846145 — MEDevices, Inc.

MEDevices, Inc. — FEI 3003067466

The FDA completed an inspection of MEDevices, Inc. on Aug 6, 2013 in Grayslake, IL. 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
Aug 6, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Grayslake, IL (United States)