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WHL-TECH ELECTRONIC CO., LIMITED

⚠️ High Risk

FEI: 3012918201 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3012918201

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Lougang, Longgang, Shenzhen, Guangdong, China

High Risk

FDA Import Risk Assessment

55.9
LowModerateHighCritical

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

Statistics

14
Total Refusals
2
Unique Violations
12/7/2023
Latest Refusal
12/7/2023
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
43.6×30%
Recency
44.0×20%
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

384214×

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.

384314×

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
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
12/7/2023
98LCA11VAPE PEN
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is WHL-TECH ELECTRONIC CO., LIMITED's FDA import refusal history?

WHL-TECH ELECTRONIC CO., LIMITED (FEI: 3012918201) has 14 FDA import refusal record(s) in our database, spanning from 12/7/2023 to 12/7/2023.

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. WHL-TECH ELECTRONIC CO., LIMITED's FEI number is 3012918201.

What types of violations has WHL-TECH ELECTRONIC CO., LIMITED received?

WHL-TECH ELECTRONIC CO., LIMITED has been cited for 2 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 WHL-TECH ELECTRONIC CO., LIMITED come from?

All FDA import refusal data for WHL-TECH ELECTRONIC CO., LIMITED 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.