FDA Inspection 634119 — EndoEvolution, LLC

EndoEvolution, LLC — FEI 3008341957

The FDA completed an inspection of EndoEvolution, LLC on Dec 4, 2009 in Wrentham, MA. 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
Dec 4, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Wrentham, MA (United States)