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HIGH VOLTAGE GROUP OY

⚠️ High Risk

FEI: 3037749350 • Jyvaskyla • FINLAND

FEI

FEI Number

3037749350

📍

Location

Jyvaskyla

🇫🇮

Country

FINLAND
🏢

Address

Ahjokatu 1416 A 14, , Jyvaskyla, , Finland

High Risk

FDA Import Risk Assessment

56.5
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
10/6/2025
Latest Refusal
8/1/2025
Earliest Refusal

Score Breakdown

Violation Severity
55.4×40%
Refusal Volume
31.3×30%
Recency
94.8×20%
Frequency
60.0×10%
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

38425×

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.

38433×

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.

35202×

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
10/6/2025
98NCA11NICOTINE POUCH
3520TP FLAVOR
Division of Southeast Imports (DSEI)
9/26/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
9/10/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
Division of Southeast Imports (DSEI)
9/4/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/29/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/1/2025
98NCA11NICOTINE POUCH
3520TP FLAVOR
3842TP NO PMTA
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HIGH VOLTAGE GROUP OY's FDA import refusal history?

HIGH VOLTAGE GROUP OY (FEI: 3037749350) has 6 FDA import refusal record(s) in our database, spanning from 8/1/2025 to 10/6/2025.

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. HIGH VOLTAGE GROUP OY's FEI number is 3037749350.

What types of violations has HIGH VOLTAGE GROUP OY received?

HIGH VOLTAGE GROUP OY 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 HIGH VOLTAGE GROUP OY come from?

All FDA import refusal data for HIGH VOLTAGE GROUP OY 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.