ImportRefusal LogoImportRefusal

NONGSHIM BUSAN FACTORY

⚠️ Moderate Risk

FEI: 3004297125 • Busan, PUSAN • SOUTH KOREA

FEI

FEI Number

3004297125

📍

Location

Busan, PUSAN

🇰🇷
🏢

Address

46 Sasang-Ro 455 Beon-Gil, Sasang-Gu, Busan, PUSAN, South Korea

Moderate Risk

FDA Import Risk Assessment

40.6
LowModerateHighCritical

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

Statistics

11
Total Refusals
8
Unique Violations
11/6/2009
Latest Refusal
5/25/2004
Earliest Refusal

Score Breakdown

Violation Severity
66.5×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
20.2×10%
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

625×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

835×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

3243×

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)).

2492×

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.

2182×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3211×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

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).

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
11/6/2009
03FGY02FLAVORED OR PARTY CRACKERS
218LIST INGRE
324NO ENGLISH
Los Angeles District Office (LOS-DO)
11/6/2009
03FGY02FLAVORED OR PARTY CRACKERS
218LIST INGRE
324NO ENGLISH
Los Angeles District Office (LOS-DO)
8/16/2006
38AGE28MIXED VEGETABLE SOUP
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/15/2005
04CGY07NOODLES, INSTANT
321LACKS N/C
324NO ENGLISH
Los Angeles District Office (LOS-DO)
8/15/2005
38CVE29VEGETABLE (SINGLE INGREDIENT NOT MENTIONED ELSEWHERE) SOUP, DRIED
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/3/2005
38AGY28MIXED VEGETABLE SOUP
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
11/30/2004
02DVF10RICE, GLUTINOUS, PROCESSED (PACKAGED)
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
11/22/2004
07YGY99SNACK FOODS NOT ELSEWHERE MENTIONED, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
8/19/2004
04CGY99NOODLES AND NOODLE PRODUCTS, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/25/2004
07AGT99BAKED SNACK FOOD, N.E.C.
249FILTHY
473LABELING
Seattle District Office (SEA-DO)
5/25/2004
07AGT99BAKED SNACK FOOD, N.E.C.
249FILTHY
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is NONGSHIM BUSAN FACTORY's FDA import refusal history?

NONGSHIM BUSAN FACTORY (FEI: 3004297125) has 11 FDA import refusal record(s) in our database, spanning from 5/25/2004 to 11/6/2009.

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. NONGSHIM BUSAN FACTORY's FEI number is 3004297125.

What types of violations has NONGSHIM BUSAN FACTORY received?

NONGSHIM BUSAN FACTORY has been cited for 8 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 NONGSHIM BUSAN FACTORY come from?

All FDA import refusal data for NONGSHIM BUSAN FACTORY 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.