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Red flags include: Selling FDA-approved medications (semaglutide, tirzepatide) under research use disclaimers this practice is what triggered enforcement actions against multiple vendors Making health claims or dosing recommendations for human use Operating without a clear US business entity or verifiable address Prior FDA warning letters (publicly searchable on the FDA website) Vendors that have built their business model around regulatory gray areas are the most vulnerable to the continued enforcement actions that characterized 2025-2026
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