SHENZHEN WEIYE ABUNDANT IMPORT A
✅ Low Risk
FEI: 3016825035 • Shenzhen • CHINA
FEI Number
3016825035
Location
Shenzhen
Country
CHINAAddress
502 Zhongxing Bld Yongx, , Shenzhen, , China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
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.
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
Frequently Asked Questions
What is SHENZHEN WEIYE ABUNDANT IMPORT A's FDA import refusal history?
SHENZHEN WEIYE ABUNDANT IMPORT A (FEI: 3016825035) has 1 FDA import refusal record(s) in our database, spanning from 6/18/2020 to 6/18/2020.
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 WEIYE ABUNDANT IMPORT A's FEI number is 3016825035.
What types of violations has SHENZHEN WEIYE ABUNDANT IMPORT A received?
SHENZHEN WEIYE ABUNDANT IMPORT A has been cited for 2 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 WEIYE ABUNDANT IMPORT A come from?
All FDA import refusal data for SHENZHEN WEIYE ABUNDANT IMPORT A 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.