The FDA introduced Good Manufacturing Practice standards to ensure that dietary supplements are free of adulterants,contaminants,and impurities and that the labels accurately depict the contents of the package.This testing in mandatory and is enforced by the FDA.

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In 2007,the GMP standards mandated that manufacturers establish quality-control procedures.The FDA introduced good Manufacturing Practice (GMP)standards in 2003 to ensure that dietary supplements are devoid of adulterants,contaminants,and impurities and that package labels accurately reflect the identity,purity,quality,and strength of the ingredients that are actually inside the package.However,testing is left to the discretion of the manufacturer,and the FDA does not inspect all manufacturing facilities for compliance.Only manufacturers that have demonstrated unsafe practices are subject to more frequent inspections.

The FDA Introduced Good Manufacturing Practice Standards to Ensure That