483 Roundup: FDA Cites Eight Firms for Quality Issues Post author:Sam Post published:May 5, 2020 Post category:Drug GMP Report The FDA found a range of quality lapses during inspections at eight U.S.-based plants. Source: Drug GMP Report You Might Also Like FDA Issues 483 to Novo Nordisk for Inadequate Sterility Controls March 8, 2016 API Maker Handed Form 483 After Failed Lab Controls and Repeat Observations February 12, 2017 FDA Denies Petition to Add Warning to Blood Thinner Labeling February 5, 2019