FDA Inspection 809572 — Uroplasty LLC

Uroplasty LLC — FEI 3002647932

The FDA completed an inspection of Uroplasty LLC on November 16, 2012 in Minnetonka, 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
November 16, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)