FDA Inspection 544391 — Uroplasty LLC

Uroplasty LLC — FEI 3002647932

The FDA completed an inspection of Uroplasty LLC on October 27, 2008 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
October 27, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minnetonka, MN (United States)

Additional Details

Postmarket Audit Inspections