Shenzhen Smoore Technology Limited
⚠️ Moderate Risk
FEI: 3009450459 • Shenzhen, Guangdong • CHINA
FEI Number
3009450459
Location
Shenzhen, Guangdong
Country
CHINAAddress
Gushu, Xixiang, F/1-F/6; Bao'An No. 16, Dongcai Industrial Zone, Shenzhen, Guangdong, 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
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.
TPLABFALSE
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 misbranded under section 903(a)(1) in that it appears that its labeling is false or misleading.
TPADFALSE
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 misbranded under section 903(a)(7) in that it appears that its advertising is false or misleading.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/14/2025 | 98LAC11VAPE PEN | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 5/14/2025 | 98LEA11VAPE PEN | 3842TP NO PMTA | Division of Southeast Imports (DSEI) |
| 4/25/2023 | 98MCA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC | 3854TPLKUSSLLB | Division of Northern Border Imports (DNBI) |
| 4/25/2023 | 98MCA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC | 3854TPLKUSSLLB | Division of Northern Border Imports (DNBI) |
| 4/25/2023 | 98MCA07ENDS CARTRIDGE | 3854TPLKUSSLLB | Division of Northern Border Imports (DNBI) |
| 4/25/2023 | 98MCA99ELECTRONIC NICOTINE DELIVERY SYSTEM COMPONENT/PART, NEC | 3854TPLKUSSLLB | Division of Northern Border Imports (DNBI) |
| 1/6/2022 | 98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC | 3889TPADFALSE | Division of Northeast Imports (DNEI) |
| 8/28/2020 | 98LAA02E-CIGARETTE, KIT | 3888TPLABFALSE | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is Shenzhen Smoore Technology Limited's FDA import refusal history?
Shenzhen Smoore Technology Limited (FEI: 3009450459) has 8 FDA import refusal record(s) in our database, spanning from 8/28/2020 to 5/14/2025.
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. Shenzhen Smoore Technology Limited's FEI number is 3009450459.
What types of violations has Shenzhen Smoore Technology Limited received?
Shenzhen Smoore Technology Limited 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 Smoore Technology Limited come from?
All FDA import refusal data for Shenzhen Smoore Technology 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.