FDA Warning Letter — TreyMed, Inc.

Case 448102 — FEI 3003007937

The FDA took a Warning Letter action against TreyMed, Inc. on January 9, 2015 (Sussex, WI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
TreyMed, Inc.
Date
January 9, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Sussex, WI (United States)