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Shenzhen Yibo Technology Co., Ltd.

⚠️ Moderate Risk

FEI: 3017209530 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3017209530

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

B Building F 7, Gongming; Guangming District Town Industrial Zone, Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

44.6
LowModerateHighCritical

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

Statistics

12
Total Refusals
5
Unique Violations
4/28/2023
Latest Refusal
9/14/2022
Earliest Refusal

Score Breakdown

Violation Severity
32.7×40%
Refusal Volume
41.3×30%
Recency
45.9×20%
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

385112×

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.

385212×

TPLACKSNC

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 in package form that appears to be misbranded under section 903(a)(2)(B) of the FD&C Act in that the label does not provide an accurate statement of the quantity of contents in terms of weight, measure or numerical count.

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.

38424×

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.

38434×

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).

Refusal History

DateProductViolationsDivision
4/28/2023
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3842TP NO PMTA
3843TP NO SE
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
4/28/2023
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3842TP NO PMTA
3843TP NO SE
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3842TP NO PMTA
3843TP NO SE
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)
9/14/2022
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3842TP NO PMTA
3843TP NO SE
3851TPLACKFIRM
3852TPLACKSNC
3854TPLKUSSLLB
Division of West Coast Imports (DWCI)

Frequently Asked Questions

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

Shenzhen Yibo Technology Co., Ltd. (FEI: 3017209530) has 12 FDA import refusal record(s) in our database, spanning from 9/14/2022 to 4/28/2023.

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 Yibo Technology Co., Ltd.'s FEI number is 3017209530.

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

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

All FDA import refusal data for Shenzhen Yibo 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.