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 EU Sets Common Specifications for Reprocessing Single-Use Devices September 11, 2020 Australia Proposes New Device Classifications to Align With EU Regs April 5, 2019 FDA Clarifies Labeling Identifier Rules for Convenience Kits May 3, 2019