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Fujian Furi Electronics Co Ltd

⚠️ Moderate Risk

FEI: 3003396478 • Wuzhou • CHINA

FEI

FEI Number

3003396478

📍

Location

Wuzhou

🇨🇳

Country

CHINA
🏢

Address

13/F Furi Mansion No169 Wuyi Rd, , Wuzhou, , China

Moderate Risk

FDA Import Risk Assessment

39.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
8/1/2013
Latest Refusal
10/15/2004
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
3.4×10%
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

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

3241×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

Refusal History

DateProductViolationsDivision
8/1/2013
04CGT10YELLOW NOODLES
11UNSAFE COL
238UNSAFE ADD
324NO ENGLISH
New York District Office (NYK-DO)
12/28/2005
23KGT05MELON SEEDS (EDIBLE SEED)
11UNSAFE COL
New York District Office (NYK-DO)
10/15/2004
24AFD13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD')
241PESTICIDE
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Fujian Furi Electronics Co Ltd's FDA import refusal history?

Fujian Furi Electronics Co Ltd (FEI: 3003396478) has 3 FDA import refusal record(s) in our database, spanning from 10/15/2004 to 8/1/2013.

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. Fujian Furi Electronics Co Ltd's FEI number is 3003396478.

What types of violations has Fujian Furi Electronics Co Ltd received?

Fujian Furi Electronics Co Ltd has been cited for 4 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 Fujian Furi Electronics Co Ltd come from?

All FDA import refusal data for Fujian Furi Electronics 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.