FDA Warning Letter — ALV Supplement Direct
The FDA took a Warning Letter action against ALV Supplement Direct on Mar 3, 2016 (Saint Paul, MN). The action was issued by CDER and concerns drugs products.
Action Details
- Facility
- ALV Supplement Direct
- Date
- Mar 3, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Center
- CDER
- Location
- Saint Paul, MN (United States)