FDA Warning Letter — Quik - N - Handi
The FDA took a Warning Letter action against Quik - N - Handi on Nov 8, 2018 (Dyersville, IA). The action was issued by CTP and concerns tobacco products.
Action Details
- Facility
- Quik - N - Handi
- Date
- Nov 8, 2018
- Fiscal Year
- 2019
- Product Type
- Tobacco
- Center
- CTP
- Location
- Dyersville, IA (United States)