The U.S. Food and Drug Administration (FDA) has posted a user-friendly document to provide information needed for successful filing of Electronic Nicotine Delivery Systems (ENDS) products.
ENDS products offered for import into the U.S. that meet the definition of a tobacco product are regulated by the FDA. In order to avoid delay of FDA admissibility determination, importers should provide the indicated information needed to their customs broker. ENDS products differing in any characteristic (including brand name, flavor, etc.) must be declared on separate FDA lines in an entry filed via ACE.
Information for successfully filing entries of Electronic Nicotine Delivery System (ENDS) Product
Related Message: CSMS# 5907442
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https://content.govdelivery.com/bulletins/gd/USDHSCBP-3878274?wgt_ref=USDHSCBP_WIDGET_2
