Inspections and Enforcement
A session from FDLI’s Introduction to Tobacco Law and Regulation
Recorded October 8, 2025
Introduction to Tobacco and Nicotine Law and Regulation: Inspections and Enforcement
Access to recordings of virtual introductory courses is limited to one year from the date of purchase as we update programs annually.
- Overview of Food, Drug, and Cosmetic Act (FDCA) inspection power
- Inspections of manufacturing facilities
- Inspections of retail establishments
- Warning letters and other enforcement tools
- Inter-agency enforcement coordination
Benjamin K. Wolf, Partner, Alston & Bird LLP
This session was recorded as part of FDLI’s Virtual Introduction to Tobacco Law and Regulation Course in October 2025.
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BENJAMIN WOLF is a Partner in the Health Care Group and a member of the Food, Drug & Device/FDA Team at Alston & Bird LLP. Ben counsels clients in many industries regulated by the Food and Drug Administration (FDA) and US Department of Agriculture (USDA). He has particular interest and experience in medical devices and agency compliance action, as well as the regulation of food, beverages, animal feed, dietary supplements, and tobacco products. In his role in industry, Ben developed medical devices, assisted with regulatory applications, and worked to address regulators’ questions. At the FDA, Ben reviewed product applications, conducted inspections, and developed policies for submission review, inspections, recalls, and other post-market issues with focuses on medical devices, combination products, and tobacco (including e-cigarettes). In private practice, Ben has worked extensively in prominent FDA regulatory firms on matters involving tobacco, food, animal feed, dietary supplements, cannabis, and cannabidiol (CBD) products.














