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MINISTRY A/S

⚠️ High Risk

FEI: 3023175411 • Svendborg, Syddanmark • DENMARK

FEI

FEI Number

3023175411

📍

Location

Svendborg, Syddanmark

🇩🇰

Country

DENMARK
🏢

Address

Gronnemosevej 6, , Svendborg, Syddanmark, Denmark

High Risk

FDA Import Risk Assessment

70.4
LowModerateHighCritical

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

Statistics

30
Total Refusals
4
Unique Violations
12/2/2025
Latest Refusal
12/4/2024
Earliest Refusal

Score Breakdown

Violation Severity
60.6×40%
Refusal Volume
55.2×30%
Recency
97.9×20%
Frequency
100.0×10%
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

384230×

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.

384314×

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).

38543×

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.

38941×

TPNICWARN

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 appears to be misbranded under section 903(a)(7)(B) in that it is sold or distributed in violation of regulations prescribed under 906(d), namely its package fails to bear the required warning statement "WARNING: This product contains nicotine. Nicotine is an addictive chemical." Or if applicable the required statement "This product is made from tobacco."

Refusal History

DateProductViolationsDivision
12/2/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
11/25/2025
98NBA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
7/14/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
7/3/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
7/3/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
7/3/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
6/26/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Northeast Imports (DNEI)
5/28/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
4/22/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/22/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/9/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/9/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/8/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
4/7/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
4/7/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
4/7/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
3/26/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
3/26/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
3/25/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
3/25/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
3/24/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
3/13/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
3894TPNICWARN
Division of Northeast Imports (DNEI)
3/11/2025
98NAA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
3/7/2025
98CDA06SNUS
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northeast Imports (DNEI)
3/6/2025
98CBA06SNUS
3842TP NO PMTA
Division of Southeast Imports (DSEI)
2/26/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
2/26/2025
98NAA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
Division of Southeast Imports (DSEI)
2/26/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
2/20/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
12/4/2024
98CCA06SNUS
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is MINISTRY A/S's FDA import refusal history?

MINISTRY A/S (FEI: 3023175411) has 30 FDA import refusal record(s) in our database, spanning from 12/4/2024 to 12/2/2025.

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. MINISTRY A/S's FEI number is 3023175411.

What types of violations has MINISTRY A/S received?

MINISTRY A/S 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 MINISTRY A/S come from?

All FDA import refusal data for MINISTRY A/S 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.