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POUCHPOINT O

⚠️ Moderate Risk

FEI: 3030261751 • Tallinn, Harju maakond • ESTONIA

FEI

FEI Number

3030261751

📍

Location

Tallinn, Harju maakond

🇪🇪

Country

ESTONIA
🏢

Address

Kivimurru Tn 18, , Tallinn, Harju maakond, Estonia

Moderate Risk

FDA Import Risk Assessment

48.6
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
3
Unique Violations
8/6/2025
Latest Refusal
7/14/2025
Earliest Refusal

Score Breakdown

Violation Severity
41.8×40%
Refusal Volume
28.8×30%
Recency
91.4×20%
Frequency
50.0×10%
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

38545×

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.

38423×

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).

Refusal History

DateProductViolationsDivision
8/6/2025
98NBA11NICOTINE POUCH
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
7/24/2025
98NBA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
7/24/2025
98NBA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
7/24/2025
98NCA11NICOTINE POUCH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
7/14/2025
98NCA11NICOTINE POUCH
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is POUCHPOINT O's FDA import refusal history?

POUCHPOINT O (FEI: 3030261751) has 5 FDA import refusal record(s) in our database, spanning from 7/14/2025 to 8/6/2025.

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. POUCHPOINT O's FEI number is 3030261751.

What types of violations has POUCHPOINT O received?

POUCHPOINT O 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 POUCHPOINT O come from?

All FDA import refusal data for POUCHPOINT O 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.