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 Targets Five Supplement Makers on Claims, Batch Production Records June 13, 2016 Spanish API Maker Lands Warning Letter for GMP Deficiencies January 17, 2017 483 Roundup: Four Facilities Rapped for Quality Deficiencies February 1, 2021