FDA Inspection 720950 — Medron, LLC

Medron, LLC — FEI 1000306216

The FDA completed an inspection of Medron, LLC on April 21, 2011 in Salt Lake City, UT. 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 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salt Lake City, UT (United States)