FDA Warning Letter — Smith & Nephew Orthopaedics GmbH
The FDA took a Warning Letter action against Smith & Nephew Orthopaedics GmbH on December 21, 2010 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Smith & Nephew Orthopaedics GmbH
- Date
- December 21, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Center
- CDRH
- Location
- Tuttlingen (Germany)