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VIKA SVENSSON GOTHENBURG

⚠️ Moderate Risk

FEI: 3035802548 • Lidkoping, Vastra Gotalands Lan • SWEDEN

FEI

FEI Number

3035802548

📍

Location

Lidkoping, Vastra Gotalands Lan

🇸🇪

Country

SWEDEN
🏢

Address

Strandgatan 28, , Lidkoping, Vastra Gotalands Lan, Sweden

Moderate Risk

FDA Import Risk Assessment

45.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
3
Unique Violations
12/29/2025
Latest Refusal
12/29/2025
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
17.7×30%
Recency
99.4×20%
Frequency
20.0×10%
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

38422×

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.

38432×

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.

Refusal History

DateProductViolationsDivision
12/29/2025
98CCA06SNUS
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northeast Imports (DNEI)
12/29/2025
98CCA06SNUS
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is VIKA SVENSSON GOTHENBURG's FDA import refusal history?

VIKA SVENSSON GOTHENBURG (FEI: 3035802548) has 2 FDA import refusal record(s) in our database, spanning from 12/29/2025 to 12/29/2025.

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. VIKA SVENSSON GOTHENBURG's FEI number is 3035802548.

What types of violations has VIKA SVENSSON GOTHENBURG received?

VIKA SVENSSON GOTHENBURG has been cited for 3 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 VIKA SVENSSON GOTHENBURG come from?

All FDA import refusal data for VIKA SVENSSON GOTHENBURG 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.