483 Roundup: FDA Flags Six Device Firms for GMP, Other Deficiencies Post author:Sam Post published:September 12, 2017 Post category:The GMP Letter The FDA found a wide range of GMP and other violations during inspections of six devicemakers. Source: The GMP Letter You Might Also Like Device Consortium Requests Feedback on Real-World Evidence Framework for IVDs June 4, 2020 FDA Moves to Improve Mammography Quality Standards April 5, 2019 CDRH Warns of Device Shortages Following Sterilizer’s Suspension April 5, 2019