SHENZHEN GREENSUN TECHNOLOGY
⚠️ Moderate Risk
FEI: 3015629640 • Shenzhen • CHINA
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/1/2023 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Northern Border Imports (DNBI) | |
| 5/14/2021 | 98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Southeast Imports (DSEI) | |
| 3/24/2021 | 98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SHENZHEN GREENSUN TECHNOLOGY's FDA import refusal history?
SHENZHEN GREENSUN TECHNOLOGY (FEI: 3015629640) has 3 FDA import refusal record(s) in our database, spanning from 3/24/2021 to 5/1/2023.
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. SHENZHEN GREENSUN TECHNOLOGY's FEI number is 3015629640.
What types of violations has SHENZHEN GREENSUN TECHNOLOGY received?
SHENZHEN GREENSUN TECHNOLOGY has been cited for 4 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 SHENZHEN GREENSUN TECHNOLOGY come from?
All FDA import refusal data for SHENZHEN GREENSUN TECHNOLOGY 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.