The FDA issues Warning Letters to provide individuals and companies with an opportunity to take voluntary and prompt corrective actions for violations of regulatory significance that may otherwise lead to enforcement.  A Warning Letter is the FDA’s principal means of achieving prompt voluntary compliance with the Federal Food, Drug, and Cosmetic Act (“FDCA”).

Below is a brief synopsis of FDA’s food-related Warning Letters issued and posted between December 16, 2013 and January 17, 2014. More information can be found here.