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KANGERTECH TECH CO LTD

⚠️ High Risk

FEI: 3021195990 • Shenzhen • CHINA

FEI

FEI Number

3021195990

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

No 8 Industrial 2nd Rd, , Shenzhen, , China

High Risk

FDA Import Risk Assessment

59.1
LowModerateHighCritical

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

Statistics

16
Total Refusals
3
Unique Violations
4/2/2025
Latest Refusal
4/2/2025
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
45.6×30%
Recency
84.0×20%
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

384216×

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.

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).

385416×

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
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is KANGERTECH TECH CO LTD's FDA import refusal history?

KANGERTECH TECH CO LTD (FEI: 3021195990) has 16 FDA import refusal record(s) in our database, spanning from 4/2/2025 to 4/2/2025.

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. KANGERTECH TECH CO LTD's FEI number is 3021195990.

What types of violations has KANGERTECH TECH CO LTD received?

KANGERTECH TECH CO LTD 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 KANGERTECH TECH CO LTD come from?

All FDA import refusal data for KANGERTECH TECH CO LTD 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.