FDA Warning Letter — Artivion, Inc
The FDA took a Warning Letter action against Artivion, Inc on January 29, 2013 (Kennesaw, GA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Artivion, Inc
- Date
- January 29, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Kennesaw, GA (United States)