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Within the last 10 years, the FDA has chronicled manufacturing problems including mislabeling of childrens tablets, where packages of the product listed an incorrect amount of the ingredients per tablet, inadequate cleaning of equipment used for manufacturing, insufficient follow-up in investigating consumer complaints, product mix-ups, and contamination with metal fragments and bacteria

Manufacturers of sterile products and any organization auditing a sterile manufacturing partner should treat this as a prompt to review environmental monitoring programs and sporicidal cleaning protocols now, ahead of any formal regulatory update

Nevertheless, the possibility of selective reporting cannot be excluded

They also provide a decent amount of fiber