ImportRefusal LogoImportRefusal

NICOBIT MB IF FACTORY

⚠️ High Risk

FEI: 3030464485 • Krakes, Kaunas County • LITHUANIA

FEI

FEI Number

3030464485

📍

Location

Krakes, Kaunas County

🇱🇹

Country

LITHUANIA
🏢

Address

Krates, P. Luksio G. 7, Krakes, Kaunas County, Lithuania

High Risk

FDA Import Risk Assessment

54.7
LowModerateHighCritical

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

Statistics

6
Total Refusals
3
Unique Violations
5/27/2025
Latest Refusal
4/7/2025
Earliest Refusal

Score Breakdown

Violation Severity
54.6×40%
Refusal Volume
31.3×30%
Recency
87.5×20%
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

38426×

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.

38435×

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
5/27/2025
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
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/22/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
4/14/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
4/7/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is NICOBIT MB IF FACTORY's FDA import refusal history?

NICOBIT MB IF FACTORY (FEI: 3030464485) has 6 FDA import refusal record(s) in our database, spanning from 4/7/2025 to 5/27/2025.

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. NICOBIT MB IF FACTORY's FEI number is 3030464485.

What types of violations has NICOBIT MB IF FACTORY received?

NICOBIT MB IF FACTORY 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 NICOBIT MB IF FACTORY come from?

All FDA import refusal data for NICOBIT MB IF FACTORY 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.