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 Inservco Inc. Receives Form 483 Citing Procedures, Device History January 18, 2017 IMDRF Opens Consultations on AERs, Principles for Labeling and UDIs August 3, 2018 Brazil Adopts Risk-Based Approach to Inspections May 4, 2017