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 FDA Will Issue Tougher Validation Requirements for Reusable Devices July 10, 2017 Chinese Medical Equipment Barred From Import by FDA September 12, 2017 FDA Details ASCA Pilot Program for Devices in New Guidance October 8, 2020