FDA Inspection 732926 — UreSil LLC

UreSil LLC — FEI 1450395

The FDA completed an inspection of UreSil LLC on Jun 30, 2011 in Skokie, IL. 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
Jun 30, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Skokie, IL (United States)