MB EUROLIT EU
⚠️ High Risk
FEI: 3037285316 • Vilnius, Vilnius County • LITHUANIA
FEI Number
3037285316
Location
Vilnius, Vilnius County
Country
LITHUANIAAddress
Vilkpedes G 20a, , Vilnius, Vilnius County, Lithuania
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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.
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/29/2025 | 98NCA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 8/29/2025 | 98NCA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 8/22/2025 | 98NCA11NICOTINE POUCH | Division of Southeast Imports (DSEI) | |
| 8/21/2025 | 98NCA11NICOTINE POUCH | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is MB EUROLIT EU's FDA import refusal history?
MB EUROLIT EU (FEI: 3037285316) has 4 FDA import refusal record(s) in our database, spanning from 8/21/2025 to 8/29/2025.
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. MB EUROLIT EU's FEI number is 3037285316.
What types of violations has MB EUROLIT EU received?
MB EUROLIT EU 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 MB EUROLIT EU come from?
All FDA import refusal data for MB EUROLIT EU 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.