FDA Inspection 642565 — ConMed Corporation

ConMed Corporation — FEI 3004491689

The FDA completed an inspection of ConMed Corporation on January 27, 2010 in Greenwood Village, CO. 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
January 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Greenwood Village, CO (United States)