FDA Hits Aesica Over Quality Controls, Record-Keeping Post author:Sam Post published:April 19, 2017 Post category:Drug Industry Daily The FDA has cited contract manufacturer Aesica for quality and record-keeping problems. Source: Drug Industry Daily You Might Also Like U.S. Bioservices Settles Novartis Kickback Case August 23, 2017 FDA Slaps Lupin With Form 483 for Risk of Contamination, Lack of In-Process Testing August 30, 2022 FDA Shares Latest Thinking on Electronic Systems, Signatures and Records in Trials March 14, 2023