FDA Inspection 605628 — Lexion Medical Llc

Lexion Medical Llc — FEI 3003631551

The FDA completed an inspection of Lexion Medical Llc on August 7, 2009 in Saint Paul, MN. 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
August 7, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)