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The Food and Drug Administration has tried to rein in tobacco companies since the 1990s, but failed to successfully enact any laws controlling tobacco marketing until five years ago, when Congress explicitly outlined the agency's power in the Family Smoking and Tobacco Control Act of 2009

Read MoreLess Tobacco Law Blog Providing timely analysis and perspectives on recent changes in the law, upcoming regulatory deadlines, and significant judicial opinions that may impact your business Representative Matters Guide clients on FDA requirements, including premarket tobacco authorization strategies and compliance with marketing orders disputes in respect of marketing denial orders, warning letters, ingredient listings, inspections, recalls, quality control, tobacco product manufacturing practices, marketing compliance, and strategies regarding FDA enforcement against unlawful actors