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Ottogi Anyang Factory

⚠️ Moderate Risk

FEI: 3005390512 • Anyang, Kyonggi • SOUTH KOREA

FEI

FEI Number

3005390512

📍

Location

Anyang, Kyonggi

🇰🇷
🏢

Address

Pyongchondong 160, , Tongan , Anyang, Kyonggi, South Korea

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

23
Total Refusals
7
Unique Violations
9/12/2012
Latest Refusal
4/16/2002
Earliest Refusal

Score Breakdown

Violation Severity
63.6×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
22.1×10%
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

8317×

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.

3246×

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)).

624×

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).

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.

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.

2601×

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.

2561×

INCONSPICU

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
9/12/2012
37JEE23CURRY SAUCE
324NO ENGLISH
328USUAL NAME
Division of Northeast Imports (DNEI)
9/12/2012
37JEE23CURRY SAUCE
218LIST INGRE
324NO ENGLISH
328USUAL NAME
Division of Northeast Imports (DNEI)
5/18/2012
37JEE23CURRY SAUCE
324NO ENGLISH
Atlanta District Office (ATL-DO)
5/18/2012
28JGT99MIXED SPICES AND SEASONING WITH SALT, N.E.C.
324NO ENGLISH
Atlanta District Office (ATL-DO)
12/28/2006
37JDT99SAUCES, N.E.C.
62NEEDS FCE
New York District Office (NYK-DO)
11/16/2004
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
256INCONSPICU
260FALSE
Seattle District Office (SEA-DO)
3/24/2004
37JCT99SAUCES, N.E.C.
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
6/11/2003
37JCP99SAUCES, N.E.C.
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/11/2003
37JCE17BEAN, GROUND SAUCE
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/11/2003
37JCE99SAUCES, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/11/2003
38CHE09CEREAL GRAIN SOUP, DRIED
83NO PROCESS
Los Angeles District Office (LOS-DO)
6/11/2003
37JGE23CURRY SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/28/2003
28FEE04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT
83NO PROCESS
Baltimore District Office (BLT-DO)
4/28/2003
37BEE32BEAN CURD, N.E.C. (MULTIPLE FOOD SPECIALTIES, SIDE DISHES & DESSERTS)
83NO PROCESS
Baltimore District Office (BLT-DO)
4/28/2003
28FGT04CURRY POWDER, GROUND, CRACKED, WITHOUT SALT
83NO PROCESS
Baltimore District Office (BLT-DO)
4/28/2003
37JGT16BEAN, BLACK SAUCE
83NO PROCESS
Baltimore District Office (BLT-DO)
2/25/2003
37JGE23CURRY SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
12/6/2002
37JCE99SAUCES, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
12/6/2002
38CHE09CEREAL GRAIN SOUP, DRIED
83NO PROCESS
Los Angeles District Office (LOS-DO)
12/6/2002
38CHE09CEREAL GRAIN SOUP, DRIED
83NO PROCESS
Los Angeles District Office (LOS-DO)
12/6/2002
37JGE23CURRY SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
04CGT07NOODLES, INSTANT
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/16/2002
38CHH09CEREAL GRAIN SOUP, DRIED
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Ottogi Anyang Factory's FDA import refusal history?

Ottogi Anyang Factory (FEI: 3005390512) has 23 FDA import refusal record(s) in our database, spanning from 4/16/2002 to 9/12/2012.

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. Ottogi Anyang Factory's FEI number is 3005390512.

What types of violations has Ottogi Anyang Factory received?

Ottogi Anyang Factory has been cited for 7 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 Ottogi Anyang Factory come from?

All FDA import refusal data for Ottogi Anyang 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.