SMOGENSNUS AB

FDA establishment 3042953818, Sweden. Every inspection FDA has posted for the site, with its outcome and cited regulations, and the shipments FDA refused at the border.

Inspections: 0
Official action indicated: 0
Last inspection ended: —
Warning letters: 0
Import refusals since 2024: 97

Inspections

0 inspections, newest first

FDA has posted no inspections for this site.

Import Refusals

97 refused shipment lines since 2024, grouped by product and charges


NICOTINE POUCHTobacco · 98NCA11	Tobacco product without a marketing order	Oct 23, 202617 lines
SMOKELESS TOBACCO POUCHESTobacco · 98CBA16	Tobacco product without a marketing orderTobacco product not reported to FDA	Oct 23, 202616 lines
SMOKELESS TOBACCO POUCHESTobacco · 98CBA16	Tobacco product without a marketing order	Oct 21, 20268 lines
NICOTINE DELIVERY PRODUCT, NECTobacco · 98NCA99	Tobacco product without a marketing orderTobacco product not reported to FDA	Oct 21, 20267 lines
SNUSTobacco · 98CCA06	Tobacco product without a marketing orderTobacco product not reported to FDA	Oct 21, 2026
NICOTINE POUCHTobacco · 98NCA11	Tobacco product without a marketing orderTobacco product not reported to FDA	Oct 20, 202640 lines
NICOTINE POUCHTobacco · 98NBA11	Tobacco product without a marketing orderTobacco product not reported to FDA	Sep 2, 20262 lines
NICOTINE POUCHTobacco · 98NBA11	Tobacco product without a marketing orderTobacco product not reported to FDATobacco label lacks "sale only allowed in the U.S."	Aug 27, 20264 lines
NICOTINE POUCHTobacco · 98NCA11	Tobacco product without a marketing orderTobacco product not reported to FDATobacco label lacks "sale only allowed in the U.S."	May 5, 2026
NICOTINE POUCHTobacco · 98NCA11	Tobacco label lacks "sale only allowed in the U.S."	Feb 21, 2026

Identifiers

FEI number: 3042953818
FDA firm profile: Data Dashboard

An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. Recalls come from FDA's enforcement reports (iRES), one row per recall even when it covers many lots. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard, warning letters and enforcement reports