FDA Warning Letter — Stryker Corporation

Case 388982 — FEI 1811755

The FDA took a Warning Letter action against Stryker Corporation on March 6, 2013 (Portage, MI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Stryker Corporation
Date
March 6, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Portage, MI (United States)