FDA Warning Letter — Snyders

Case 538761 — FEI 3010058095

The FDA took a Warning Letter action against Snyders on Oct 5, 2017 (Duluth, MN). The action was issued by CTP and concerns tobacco products.

Action Details

Facility
Snyders
Date
Oct 5, 2017
Fiscal Year
2018
Product Type
Tobacco
Center
CTP
Location
Duluth, MN (United States)