ImportRefusal LogoImportRefusal

SHENZHEN AIRIS ELECTRONIC CO

⚠️ Moderate Risk

FEI: 3020054648 • Shenzhen • CHINA

FEI

FEI Number

3020054648

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

1 Fuhai St, Tangwei Com, 2 Building, Fucheng Industrial, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

43.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/7/2023
Latest Refusal
12/7/2023
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
57.6×20%
Frequency
10.0×10%
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

38421×

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.

Refusal History

DateProductViolationsDivision
12/7/2023
98LCA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3842TP NO PMTA
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is SHENZHEN AIRIS ELECTRONIC CO's FDA import refusal history?

SHENZHEN AIRIS ELECTRONIC CO (FEI: 3020054648) has 1 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 AIRIS ELECTRONIC CO's FEI number is 3020054648.

What types of violations has SHENZHEN AIRIS ELECTRONIC CO received?

SHENZHEN AIRIS ELECTRONIC 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 AIRIS ELECTRONIC CO come from?

All FDA import refusal data for SHENZHEN AIRIS ELECTRONIC 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.