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Xiamen Kingdomway Group Company

⚠️ Moderate Risk

FEI: 3008086862 • Xiamen, Fujian • CHINA

FEI

FEI Number

3008086862

📍

Location

Xiamen, Fujian

🇨🇳

Country

CHINA
🏢

Address

NO. 299 West Yangguang Road, Xingyang Insutrial Area, Xiamen, Fujian, China

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
7/27/2017
Latest Refusal
7/27/2017
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
7/27/2017
54YCZ99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
249FILTHY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Xiamen Kingdomway Group Company's FDA import refusal history?

Xiamen Kingdomway Group Company (FEI: 3008086862) has 1 FDA import refusal record(s) in our database, spanning from 7/27/2017 to 7/27/2017.

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. Xiamen Kingdomway Group Company's FEI number is 3008086862.

What types of violations has Xiamen Kingdomway Group Company received?

Xiamen Kingdomway Group Company 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 Xiamen Kingdomway Group Company come from?

All FDA import refusal data for Xiamen Kingdomway Group Company 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.