FDA Warning Letter — Stryker Craniomaxillofacial Division
The FDA took a Warning Letter action against Stryker Craniomaxillofacial Division on May 5, 2009 (Portage, MI). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.
Action Details
- Facility
- Stryker Craniomaxillofacial Division
- Date
- May 5, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Center
- CDRH
- Location
- Portage, MI (United States)