viernes, 25 de octubre de 2019

FDA In Brief: FDA notifies Eonsmoke LLC to remove nearly 100 flavored electronic nicotine delivery system products from the market for not having required marketing authorization, among other violations



FDA In Brief: FDA notifies Eonsmoke LLC to remove nearly 100 flavored electronic nicotine delivery system products from the market for not having required marketing authorization, among other violations 

Today, the U.S. Food and Drug Administration issued a warning letter to Eonsmoke LLC (Eonsmoke) of Clifton, New Jersey, notifying the company that nearly 100 flavored electronic nicotine delivery system (ENDS) products do not have the required marketing authorization, and thus cannot be legally sold in the United States, among other violations.

Eonsmoke sells ENDS products, such as flavored e-liquids, many of which are compatible with other popular ENDS devices, such as JUUL. This warning letter follows a previous letter from the FDA to Eonsmoke requesting additional information about whether Eonsmoke was illegally marketing new tobacco products without ...

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