Guidance for Reviewers on Repeal of Section 507 of the Federal Food, Drug, and Cosmetic Act; Availability

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The Food and Drug Administration (FDA) is announcing the availability of a guidance document for reviewers entitled ``Repeal of Section 507 of the Federal Food, Drug, and Cosmetic Act.'' The guidance is intended to clarify the administrative processes that will be followed in implementing the Food and Drug Administration Modernization Act of 1997 (the FDAMA).