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The FDA concluded that the company's manufacturing systems, laboratory controls, and quality oversight failed to comply with Current Good Manufacturing Practice (CGMP) requirements, ultimately classifying products manufactured at the facility as adulterated under the Federal Food, Drug, and Cosmetic Actnot because contamination was confirmed, but because the quality systems could no longer be relied upon

Twice-weekly dosing reduces protocol complexity and cumulative handling risk while achieving identical systemic exposure

Rhonda: because, let me tell you, 400 IUs of vitamin D aint much