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The FDA will review the full meeting record After the meeting, the FDA can consider: The committee’s recommendations Written comments submitted to the public docket Public testimony presented during the meeting FDA staff evaluations Substance characterization and sourcing concerns Available human, animal, and laboratory research Additional regulatory or safety information The FDA’s July 2026 briefing document states that the final determination may also be affected by issues that were not discussed during the public meeting

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When an individual doesn’t get adequate amounts of vitamin B12, the myelin sheath, or protective covering that envelops the nerves, sustains damage