FDA Warning Letter — ConMed Corporation

Case 414800 — FEI 3004491689

The FDA took a Warning Letter action against ConMed Corporation on January 29, 2014 (Greenwood Village, CO). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
ConMed Corporation
Date
January 29, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Greenwood Village, CO (United States)