FDA Inspection 1054426 — EndoEvolution, LLC

EndoEvolution, LLC — FEI 3008341957

The FDA completed an inspection of EndoEvolution, LLC on May 7, 2018 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
May 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wrentham, MA (United States)