FDA Warning Letter — 8046255 Canada Inc. DBA Viatrexx
The FDA took a Warning Letter action against 8046255 Canada Inc. DBA Viatrexx on June 11, 2020 (Beloeil, Canada). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- 8046255 Canada Inc. DBA Viatrexx
- Date
- June 11, 2020
- Fiscal Year
- 2020
- Product Type
- Drugs
- Center
- CDER
- Location
- Beloeil (Canada)