Federal Register Notice: FDA’s proposed collection of information, “Requests for Inspection Under the Inspection by Accredited Persons Program — 21 U.S.C. 374(g),” has been submitted to the Office of Management and Budget for review and clearance under the Paperwork Reduction Act of 1995. The Accredited Persons program applies to manufacturers who currently market their medical devices in the U.S. and who also market or plan to market their devices in foreign countries. To view this notice, click here.