SHENZHEN FUNYIN ELETRONIC TECHNOLOGY CO LTD

⚠️ High Risk

FEI: 3024353729 • Shenzhen • CHINA

FEI

FEI Number

3024353729

📍

Location

Shenzhen

🇨🇳

Country

CHINA

🏢

Address

And 401 Bldg A, 205 Fuhai Street; Fuyuan Industrial Zone, Shenzhen, , China

High Risk

FDA Import Risk Assessment

54.3

LowModerateHighCritical

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

Statistics

Total Refusals

Unique Violations

6/22/2023

Latest Refusal

3/21/2023

Earliest Refusal

Score Breakdown

Violation Severity

62.5×40%

Refusal Volume

41.3×30%

Recency

34.8×20%

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

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.

38432×

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.

Refusal History

Date	Product	Violations	Division
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
6/22/2023	98LCA11VAPE PEN	3842TP NO PMTA	Division of West Coast Imports (DWCI)
3/21/2023	98MCA01E-LIQUID	3842TP NO PMTA 3843TP NO SE 3851TPLACKFIRM	Division of West Coast Imports (DWCI)
3/21/2023	98MCA01E-LIQUID	3842TP NO PMTA 3843TP NO SE 3851TPLACKFIRM	Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is SHENZHEN FUNYIN ELETRONIC TECHNOLOGY CO LTD's FDA import refusal history?

SHENZHEN FUNYIN ELETRONIC TECHNOLOGY CO LTD (FEI: 3024353729) has 12 FDA import refusal record(s) in our database, spanning from 3/21/2023 to 6/22/2023.

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 FUNYIN ELETRONIC TECHNOLOGY CO LTD's FEI number is 3024353729.

What types of violations has SHENZHEN FUNYIN ELETRONIC TECHNOLOGY CO LTD received?

SHENZHEN FUNYIN ELETRONIC 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 FUNYIN ELETRONIC TECHNOLOGY CO LTD come from?

All FDA import refusal data for SHENZHEN FUNYIN ELETRONIC 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.