FDA News: The FDA released its June, 2011 Draft Guidance documents for two matters: (i) Guidance for Industry and Staff: Classification of Products as Drugs and Devices & Additional Product Classification Issues, and (ii) Guidance for Industry and Staff: Interpretation of the Term "Chemical Action" in the Definition of Device under Section 201(h) of the Federal Food, Drug and Cosmetic Act.  Comments are due within 90 days of publication in the Federal Register.