Short answer: CardioFlush is manufactured in an FDA-registered facility following Good Manufacturing Practices; this does not mean the product itself has been evaluated or approved by the FDA.
Why this distinction is stated so directly
This phrasing deliberately separates facility registration and manufacturing standards from product approval — two genuinely different regulatory concepts worth understanding clearly.
What "FDA-registered facility" specifically means
It means the manufacturing location meets certain federal standards — it does not mean the FDA has reviewed or endorsed CardioFlush's specific cardiovascular claims.
💡 Worth knowing: these statements have not been evaluated by the Food and Drug Administration — a direct, standard disclosure worth reading alongside this facility-registration clarification.
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