FDA Inspection 805892 — Medfaxx, Inc.

Medfaxx, Inc. — FEI 3001451345

The FDA completed an inspection of Medfaxx, Inc. on November 2, 2012 in Wake Forest, NC. 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
November 2, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wake Forest, NC (United States)