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Shenzhen Weisigu Technology Co., Ltd

⚠️ High Risk

FEI: 3032956374 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3032956374

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Zhonghengsheng High-Tech Park, No. 3 Xinyu Road, Shajing Street, Shenzhen, Guangdong, China

High Risk

FDA Import Risk Assessment

53.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

12
Total Refusals
3
Unique Violations
12/2/2024
Latest Refusal
12/2/2024
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
41.3×30%
Recency
63.8×20%
Frequency
100.0×10%
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

384212×

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.

384312×

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).

385412×

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.

Refusal History

DateProductViolationsDivision
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
12/2/2024
98LCA03E-HOOKAH
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is Shenzhen Weisigu Technology Co., Ltd's FDA import refusal history?

Shenzhen Weisigu Technology Co., Ltd (FEI: 3032956374) has 12 FDA import refusal record(s) in our database, spanning from 12/2/2024 to 12/2/2024.

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 Weisigu Technology Co., Ltd's FEI number is 3032956374.

What types of violations has Shenzhen Weisigu Technology Co., Ltd received?

Shenzhen Weisigu 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 Shenzhen Weisigu Technology Co., Ltd come from?

All FDA import refusal data for Shenzhen Weisigu 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.