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SHENZHEN OVANVAPE TECHNOLOGY CO

⚠️ High Risk

FEI: 3032972212 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3032972212

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Bldg 6f, 1 Shayi Commu S; Baoan, Shenzhen, Guangdong, China

High Risk

FDA Import Risk Assessment

53.4
LowModerateHighCritical

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

Statistics

19
Total Refusals
1
Unique Violations
4/2/2025
Latest Refusal
4/2/2025
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
48.2×30%
Recency
84.5×20%
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

385119×

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

DateProductViolationsDivision
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)
4/2/2025
98LCA01E-CIGARETTE
3851TPLACKFIRM
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is SHENZHEN OVANVAPE TECHNOLOGY CO's FDA import refusal history?

SHENZHEN OVANVAPE TECHNOLOGY CO (FEI: 3032972212) has 19 FDA import refusal record(s) in our database, spanning from 4/2/2025 to 4/2/2025.

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 OVANVAPE TECHNOLOGY CO's FEI number is 3032972212.

What types of violations has SHENZHEN OVANVAPE TECHNOLOGY CO received?

SHENZHEN OVANVAPE TECHNOLOGY CO has been cited for 1 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 OVANVAPE TECHNOLOGY CO come from?

All FDA import refusal data for SHENZHEN OVANVAPE 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.