FDA Inspection 828779 — Medifocus, Inc.

Medifocus, Inc. — FEI 3009969279

The FDA completed an inspection of Medifocus, Inc. on Apr 26, 2013 in Columbia, MD. 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
Apr 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia, MD (United States)