Federal Register Notice: FDA is releasing the criteria it will use to accredit persons for the purpose of conducting inspections of eligible device manufacturers under section 201 of the Medical Device User Fee and Modernization Act of 2002 (MDUFMA), which established an “inspection by accredited persons” program. FDA is also making available a guidance document that will provide information for those interested in participating. To download the guidance, click here. To view this notice, click here.