ImportRefusal LogoImportRefusal

SHENZHEN AVIDVAPE TECHNOLOGY CO

⚠️ High Risk

FEI: 3016258831 • Shenzhen • CHINA

FEI

FEI Number

3016258831

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Building B, Area A Jiuji, Shenzhen, , China

High Risk

FDA Import Risk Assessment

58.3
LowModerateHighCritical

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

Statistics

13
Total Refusals
1
Unique Violations
12/2/2021
Latest Refusal
12/2/2021
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
42.5×30%
Recency
17.8×20%
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

© ImportRefusal.com Original Analysis

Violation Summary

378113×

TPNOWRNLBL

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is a tobacco product which appears to be misbranded under section 903(a)(8)(B)(i) and 903(a)(1) because its package label does not include a brief statement of the relevant warnings (i.e., one of the four warnings required by section 3 of the Comprehensive Smokeless Tobacco Health Education Act).

Refusal History

DateProductViolationsDivision
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)
12/2/2021
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3781TPNOWRNLBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

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

SHENZHEN AVIDVAPE TECHNOLOGY CO (FEI: 3016258831) has 13 FDA import refusal record(s) in our database, spanning from 12/2/2021 to 12/2/2021.

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 AVIDVAPE TECHNOLOGY CO's FEI number is 3016258831.

What types of violations has SHENZHEN AVIDVAPE TECHNOLOGY CO received?

SHENZHEN AVIDVAPE 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 AVIDVAPE TECHNOLOGY CO come from?

All FDA import refusal data for SHENZHEN AVIDVAPE 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.