FDA Inspection 828460 — Conmed

Conmed — FEI 3006217371

The FDA completed an inspection of Conmed on Apr 11, 2013 in Milford, CT. 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
Apr 11, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Milford, CT (United States)