FDA Inspection 705738 — Medisurge, LLC.

Medisurge, LLC. — FEI 3004986960

The FDA completed an inspection of Medisurge, LLC. on October 4, 2010 in Grand Rapids, MI. 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
October 4, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Grand Rapids, MI (United States)