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TRIDOTS UK

⚠️ High Risk

FEI: 3035487766 • London, LND • UNITED KINGDOM

FEI

FEI Number

3035487766

📍

Location

London, LND

🇬🇧
🏢

Address

65 London Wall, , London, LND, United Kingdom

High Risk

FDA Import Risk Assessment

64.2
LowModerateHighCritical

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

Statistics

22
Total Refusals
4
Unique Violations
12/18/2025
Latest Refusal
6/12/2025
Earliest Refusal

Score Breakdown

Violation Severity
48.4×40%
Refusal Volume
50.4×30%
Recency
98.7×20%
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

384221×

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.

385417×

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.

384316×

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).

38942×

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
12/18/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
3894TPNICWARN
Division of Northeast Imports (DNEI)
12/18/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
3894TPNICWARN
Division of Northeast Imports (DNEI)
12/1/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
10/6/2025
98NBA11NICOTINE POUCH
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
9/29/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
9/11/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
9/4/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
9/4/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
9/4/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
9/4/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
9/4/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
Division of Southeast Imports (DSEI)
8/29/2025
98NCA99NICOTINE DELIVERY PRODUCT, NEC
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/27/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/26/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/11/2025
98NBA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/11/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/11/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/5/2025
98NCA11NICOTINE POUCH
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
7/28/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/20/2025
98NBA11NICOTINE POUCH
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/20/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/12/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is TRIDOTS UK's FDA import refusal history?

TRIDOTS UK (FEI: 3035487766) has 22 FDA import refusal record(s) in our database, spanning from 6/12/2025 to 12/18/2025.

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. TRIDOTS UK's FEI number is 3035487766.

What types of violations has TRIDOTS UK received?

TRIDOTS UK 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 TRIDOTS UK come from?

All FDA import refusal data for TRIDOTS UK 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.