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SHENZHEN KIMDLE TECH CO., LTD

⚠️ High Risk

FEI: 3037450053 • Shenzhen • CHINA

FEI

FEI Number

3037450053

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Lixing Commercial Building, Fenghuangshan Avenue; Baoan Dist5555, Shenzhen, , China

High Risk

FDA Import Risk Assessment

50.2
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
7/1/2025
Latest Refusal
7/1/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
89.2×20%
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
7/1/2025
98LAA99ELECTRONIC NICOTINE DELIVERY SYSTEM, NEC
3842TP NO PMTA
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is SHENZHEN KIMDLE TECH CO., LTD's FDA import refusal history?

SHENZHEN KIMDLE TECH CO., LTD (FEI: 3037450053) has 1 FDA import refusal record(s) in our database, spanning from 7/1/2025 to 7/1/2025.

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 KIMDLE TECH CO., LTD's FEI number is 3037450053.

What types of violations has SHENZHEN KIMDLE TECH CO., LTD received?

SHENZHEN KIMDLE TECH CO., LTD 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 KIMDLE TECH CO., LTD come from?

All FDA import refusal data for SHENZHEN KIMDLE TECH CO., LTD 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.