FDA Inspection 673047 — Urologix LLC

Urologix LLC — FEI 3000718675

The FDA completed an inspection of Urologix LLC on Jul 23, 2010 in Plymouth, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 23, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Plymouth, MN (United States)