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A Day In FDA Supplement Industry Regulation: Track Spiked Product, Oversee Court-Ordered Recall

This article was originally published in The Tan Sheet

Executive Summary

FDA identifies a product marketed as a supplement but labeled as containing anabolic steroids and linked to three adverse event reports about “serious liver injury,” and also notes the recall of nearly 150 supplements by a firm shut down in a consent decree made after repeated GMP violations.

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