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SILVERTON AB

⚠️ High Risk

FEI: 3016923702 • Goteborg, Vastra Gotalands Lan • SWEDEN

FEI

FEI Number

3016923702

📍

Location

Goteborg, Vastra Gotalands Lan

🇸🇪

Country

SWEDEN
🏢

Address

Saterigatan 25, , Goteborg, Vastra Gotalands Lan, Sweden

High Risk

FDA Import Risk Assessment

62.0
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

15
Total Refusals
4
Unique Violations
6/30/2025
Latest Refusal
4/25/2023
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
44.6×30%
Recency
88.9×20%
Frequency
68.7×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

384214×

TP NO PMTA

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be adulterated under section 902(6)(A) of the FD&C Act in that it does not have an FDA marketing order in effect under section 910(c)(1)(A)(i) of the FD&C Act.

38438×

TP NO SE

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be misbranded under section 903(a)(6) of the FD&C Act in that a notice or other information respecting it was not provided as required by section 905(j).

38542×

TPLKUSSLLB

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.

35201×

TP FLAVOR

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is, or purports to be or is represented as, a tobacco product that is subject to a tobacco product standard established under section 907, and violates 907 (a) (1) (A) in that the article appears to contain, as a constituent or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, that is a characterizing flavor of the tobacco product or tobacco smoke.

Refusal History

DateProductViolationsDivision
6/30/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/30/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/6/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
6/6/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
6/6/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
5/28/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
5/28/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
5/28/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
5/23/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
5/19/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
5/12/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
5/12/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
5/12/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
3/27/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/25/2023
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3520TP FLAVOR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SILVERTON AB's FDA import refusal history?

SILVERTON AB (FEI: 3016923702) has 15 FDA import refusal record(s) in our database, spanning from 4/25/2023 to 6/30/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. SILVERTON AB's FEI number is 3016923702.

What types of violations has SILVERTON AB received?

SILVERTON AB has been cited for 4 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about SILVERTON AB come from?

All FDA import refusal data for SILVERTON AB is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.