Cenova is listed as a contract manufacturer for multiple customers selling products on the US market. During week 15 a three day long FDA inspection was performed at the Cenova facility. Focus was Cenovas general quality management system (QMS). The result of the inspection was zero observations, meaning no issue of a Form 483. This is just another evidence that Cenova possess a world class QMS, which not only meets high demands from customers and market, but also meets the high regulatory requirements in FDA QSR 21CRF820.