The Sector inspector will post the final 483 to his/her superiors; In the event the findings are serious ample, or In the event the response to the 483 that you choose to post is considered inadequate, an FDA Warning Letter could possibly be issued to your firm. A Warning Letter https://franciscorktah.suomiblog.com/5-tips-about-pharmaceutical-quality-management-system-consulting-you-can-use-today-53855897