ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD
⚠️ High Risk
FEI: 3026651462 • Zhongshan City • CHINA
FEI Number
3026651462
Location
Zhongshan City
Country
CHINAAddress
No 1 Zhimei Street, Fusha, Town,Guangdong Province, Zhongshan City, , China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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.
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).
TPLACKFIRM
This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.
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.
TPLACKSNC
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 in package form that appears to be misbranded under section 903(a)(2)(B) of the FD&C Act in that the label does not provide an accurate statement of the quantity of contents in terms of weight, measure or numerical count.
TP VIOL911
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 in violation of section 911.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/2/2025 | 98LAA01E-CIGARETTE | Division of West Coast Imports (DWCI) | |
| 9/2/2025 | 98LAA01E-CIGARETTE | Division of West Coast Imports (DWCI) | |
| 9/2/2025 | 98LAA01E-CIGARETTE | Division of West Coast Imports (DWCI) | |
| 6/6/2025 | 98LAA01E-CIGARETTE | 3580TP VIOL911 | Division of West Coast Imports (DWCI) |
| 5/31/2024 | 98MEA04ENDS BATTERY | Division of West Coast Imports (DWCI) | |
| 5/31/2024 | 98MCA07ENDS CARTRIDGE | Division of West Coast Imports (DWCI) | |
| 5/19/2023 | 98LCA05E-CIGAR | Division of Southeast Imports (DSEI) | |
| 4/28/2023 | 98LCA01E-CIGARETTE | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD's FDA import refusal history?
ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD (FEI: 3026651462) has 8 FDA import refusal record(s) in our database, spanning from 4/28/2023 to 9/2/2025.
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. ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD's FEI number is 3026651462.
What types of violations has ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD received?
ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD has been cited for 6 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 ZHONGSHAN HEWO ELECTRONIC TECH CO.,LTD come from?
All FDA import refusal data for ZHONGSHAN HEWO ELECTRONIC 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.