FDA Inspection 911094 — Medbio, Inc.

Medbio, Inc. — FEI 3009810261

The FDA completed an inspection of Medbio, Inc. on Jan 23, 2015 in Grand Rapids, MI. 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
Jan 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Grand Rapids, MI (United States)