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Shenzhen Kanger Technology Co

⚠️ Moderate Risk

FEI: 3009276431 • Shenzhen • CHINA

FEI

FEI Number

3009276431

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Bldg A1, 66 Hexiu Rd, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

49.0
LowModerateHighCritical

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

Statistics

7
Total Refusals
1
Unique Violations
2/2/2017
Latest Refusal
2/2/2017
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

35207×

TP FLAVOR

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is, or purports to be or is represented as, a tobacco product that is subject to a tobacco product standard established under section 907, and violates 907 (a) (1) (A) in that the article appears to contain, as a constituent or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, that is a characterizing flavor of the tobacco product or tobacco smoke.

Refusal History

DateProductViolationsDivision
2/2/2017
98MCA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)
2/2/2017
98MCA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)
2/2/2017
98MAA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)
2/2/2017
98MAA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)
2/2/2017
98MAA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)
2/2/2017
98MBA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)
2/2/2017
98MAA07ENDS CARTRIDGE
3520TP FLAVOR
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Shenzhen Kanger Technology Co's FDA import refusal history?

Shenzhen Kanger Technology Co (FEI: 3009276431) has 7 FDA import refusal record(s) in our database, spanning from 2/2/2017 to 2/2/2017.

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 Kanger Technology Co's FEI number is 3009276431.

What types of violations has Shenzhen Kanger Technology Co received?

Shenzhen Kanger 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 Kanger Technology Co come from?

All FDA import refusal data for Shenzhen Kanger 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.