FDA Warning Letter — OriGen Biomedical, Inc.
The FDA took a Warning Letter action against OriGen Biomedical, Inc. on December 20, 2018 (Austin, TX). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.
Action Details
- Facility
- OriGen Biomedical, Inc.
- Date
- December 20, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Center
- CDRH
- Location
- Austin, TX (United States)