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Shenzhen Uwell Technology

⚠️ Moderate Risk

FEI: 3012096013 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3012096013

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

3/F, Caowei First Industrial Zone, Xixiang Street, Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

49.2
LowModerateHighCritical

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

Statistics

15
Total Refusals
5
Unique Violations
4/18/2025
Latest Refusal
4/28/2020
Earliest Refusal

Score Breakdown

Violation Severity
39.6×40%
Refusal Volume
44.6×30%
Recency
84.8×20%
Frequency
30.1×10%
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

385410×

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.

38425×

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.

38435×

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).

38512×

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.

38941×

TPNICWARN

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)(B) in that it is sold or distributed in violation of regulations prescribed under 906(d), namely its package fails to bear the required warning statement "WARNING: This product contains nicotine. Nicotine is an addictive chemical." Or if applicable the required statement "This product is made from tobacco."

Refusal History

DateProductViolationsDivision
4/18/2025
98LAA02E-CIGARETTE, KIT
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
4/18/2025
98LAA02E-CIGARETTE, KIT
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
4/18/2025
98LAA02E-CIGARETTE, KIT
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
4/18/2025
98LAA02E-CIGARETTE, KIT
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
4/18/2025
98LAA02E-CIGARETTE, KIT
3842TP NO PMTA
3843TP NO SE
Division of West Coast Imports (DWCI)
2/25/2022
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
1/11/2022
98MAA10ENDS COIL
3851TPLACKFIRM
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
10/15/2021
98MAA10ENDS COIL
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
6/9/2020
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/9/2020
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
6/9/2020
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
5/20/2020
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
5/20/2020
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
5/20/2020
98MAA03ENDS ATOMIZER
3851TPLACKFIRM
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
4/28/2020
98LAA02E-CIGARETTE, KIT
3854TPLKUSSLLB
3894TPNICWARN
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Shenzhen Uwell Technology's FDA import refusal history?

Shenzhen Uwell Technology (FEI: 3012096013) has 15 FDA import refusal record(s) in our database, spanning from 4/28/2020 to 4/18/2025.

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 Uwell Technology's FEI number is 3012096013.

What types of violations has Shenzhen Uwell Technology received?

Shenzhen Uwell Technology has been cited for 5 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 Uwell Technology come from?

All FDA import refusal data for Shenzhen Uwell 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.