Federal Register Notice: FDA seeks public comment on the publication of the criteria it intends to use to accredit third parties to conduct inspections of eligible manufacturers of Class 2 or Class 3 medical devices. Comments should be submitted by 12/21. The agency has a guidance document with information for those interested in participating in this program, Implementation of the Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002; Accreditation Criteria. To view this notice, click here.