Shenzhen Fango Technology Co
⚠️ High Risk
FEI: 3027873599 • Shajing Guangdong • CHINA
FEI Number
3027873599
Location
Shajing Guangdong
Country
CHINAAddress
B Building, Zhongxinmingzuo building Bhaoxiang Road, Shajing Guangdong, , China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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.
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).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) | |
| 12/7/2023 | 98LCA11VAPE PEN | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Shenzhen Fango Technology Co's FDA import refusal history?
Shenzhen Fango Technology Co (FEI: 3027873599) has 10 FDA import refusal record(s) in our database, spanning from 12/7/2023 to 12/7/2023.
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 Fango Technology Co's FEI number is 3027873599.
What types of violations has Shenzhen Fango Technology Co received?
Shenzhen Fango Technology Co has been cited for 4 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 Fango Technology Co come from?
All FDA import refusal data for Shenzhen Fango Technology Co 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.