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Shenzhen COEUS Technology Co., LTD.

⚠️ Moderate Risk

FEI: 3028943120 • Shenzhen • CHINA

FEI

FEI Number

3028943120

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

511, Building 3, Baoxing Zhihui City, Zhoushi Road, Bao'an District, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

39.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
8/28/2024
Latest Refusal
8/28/2024
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
22.3×30%
Recency
57.5×20%
Frequency
30.0×10%
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

38423×

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.

38433×

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).

38543×

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
8/28/2024
98MEA03ENDS ATOMIZER
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
8/28/2024
98MEA03ENDS ATOMIZER
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)
8/28/2024
98MEA03ENDS ATOMIZER
3842TP NO PMTA
3843TP NO SE
3854TPLKUSSLLB
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Shenzhen COEUS Technology Co., LTD.'s FDA import refusal history?

Shenzhen COEUS Technology Co., LTD. (FEI: 3028943120) has 3 FDA import refusal record(s) in our database, spanning from 8/28/2024 to 8/28/2024.

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 COEUS Technology Co., LTD.'s FEI number is 3028943120.

What types of violations has Shenzhen COEUS Technology Co., LTD. received?

Shenzhen COEUS 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 COEUS Technology Co., LTD. come from?

All FDA import refusal data for Shenzhen COEUS 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.