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BEON YOUNG PRODUCE

⚠️ Moderate Risk

FEI: 3009000448 • PUSAN, KR-26 • SOUTH KOREA

FEI

FEI Number

3009000448

📍

Location

PUSAN, KR-26

🇰🇷
🏢

Address

334-4 NAM SAN DONG, KEUM JANG GU, PUSAN, KR-26, South Korea

Moderate Risk

FDA Import Risk Assessment

32.1
LowModerateHighCritical

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

Statistics

5
Total Refusals
6
Unique Violations
11/26/2019
Latest Refusal
12/7/2011
Earliest Refusal

Score Breakdown

Violation Severity
57.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
6.3×10%
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

2382×

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.

2602×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3242×

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)).

3282×

USUAL NAME

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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

111×

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).

641×

YELLOW #5

The food appears to bear or contain the color additive FD & C Yellow No. 5, which is not declared on the label per 21 CFR 74.705(a)(c) under section 721.

Refusal History

DateProductViolationsDivision
11/26/2019
02FGN99WHEAT, MILLED PRODUCT, N.E.C.
260FALSE
324NO ENGLISH
328USUAL NAME
Division of West Coast Imports (DWCI)
11/26/2019
02FGN99WHEAT, MILLED PRODUCT, N.E.C.
260FALSE
324NO ENGLISH
328USUAL NAME
Division of West Coast Imports (DWCI)
10/4/2012
03FHT99CRACKERS (NON FILLED) N.E.C.
238UNSAFE ADD
Los Angeles District Office (LOS-DO)
2/14/2012
03FHT99CRACKERS (NON FILLED) N.E.C.
238UNSAFE ADD
Los Angeles District Office (LOS-DO)
12/7/2011
03FHT99CRACKERS (NON FILLED) N.E.C.
11UNSAFE COL
64YELLOW #5
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is BEON YOUNG PRODUCE's FDA import refusal history?

BEON YOUNG PRODUCE (FEI: 3009000448) has 5 FDA import refusal record(s) in our database, spanning from 12/7/2011 to 11/26/2019.

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. BEON YOUNG PRODUCE's FEI number is 3009000448.

What types of violations has BEON YOUNG PRODUCE received?

BEON YOUNG PRODUCE has been cited for 6 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 BEON YOUNG PRODUCE come from?

All FDA import refusal data for BEON YOUNG PRODUCE 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.