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 Warning Letter Roundup: FDA Warns Devicemakers in India, Lithuania, Texas January 18, 2018 FDA Classifies Humidified Oxygen Devices, Assigns Special Controls November 8, 2018 Tips for Upgrading Your Medical Device Recall Strategy September 11, 2020