FDA Inspection 779339 — Medge Platforms, Inc.

Medge Platforms, Inc. — FEI 3003381802

The FDA completed an inspection of Medge Platforms, Inc. on April 24, 2012 in New York, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 24, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
New York, NY (United States)