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DONGGUAN YIHAI TECHNOLOGY CO., LTD

⚠️ Moderate Risk

FEI: 3038358828 • Dong Guan, Guangdong • CHINA

FEI

FEI Number

3038358828

📍

Location

Dong Guan, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Nancheng Gongyequ Room 302, No.35 Yunchen Park Xinghong Road; Daojiaozhen, Dong Guan, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

46.1
LowModerateHighCritical

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

Statistics

5
Total Refusals
3
Unique Violations
8/4/2025
Latest Refusal
7/29/2025
Earliest Refusal

Score Breakdown

Violation Severity
42.9×40%
Refusal Volume
28.8×30%
Recency
76.7×20%
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

38543×

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.

38422×

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.

38432×

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
8/4/2025
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
8/4/2025
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
8/4/2025
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
7/29/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
Division of Northern Border Imports (DNBI)
7/29/2025
98LCA01E-CIGARETTE
3842TP NO PMTA
3843TP NO SE
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is DONGGUAN YIHAI TECHNOLOGY CO., LTD's FDA import refusal history?

DONGGUAN YIHAI TECHNOLOGY CO., LTD (FEI: 3038358828) has 5 FDA import refusal record(s) in our database, spanning from 7/29/2025 to 8/4/2025.

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. DONGGUAN YIHAI TECHNOLOGY CO., LTD's FEI number is 3038358828.

What types of violations has DONGGUAN YIHAI TECHNOLOGY CO., LTD received?

DONGGUAN YIHAI TECHNOLOGY 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 DONGGUAN YIHAI TECHNOLOGY CO., LTD come from?

All FDA import refusal data for DONGGUAN YIHAI TECHNOLOGY 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.