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RUO designation means: Not reviewed or approved for human administration by the FDA No legal claims about safety, efficacy, or therapeutic intent Manufacturer avoids clinical liability Yet it does not inherently mean: Low purity Contamination Inferior synthesis Unsafe chemistry The real danger you correctly highlight is unverified sourcing: Non-registered facilities No GMP discipline No validated cleaning protocols No batch traceability No endotoxin controls No sterility assurance level (SAL) I believe: Regulatory status is being confused with chemical reality

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