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Ottogi SF Corporation

⚠️ Moderate Risk

FEI: 2000003327 • Goseong, Gyeongsangnam • SOUTH KOREA

FEI

FEI Number

2000003327

📍

Location

Goseong, Gyeongsangnam

🇰🇷
🏢

Address

2771 Namhaeandae-Ro, Goseong-Eupkorea, Goseong, Gyeongsangnam, South Korea

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

10
Total Refusals
4
Unique Violations
9/12/2012
Latest Refusal
3/11/2002
Earliest Refusal

Score Breakdown

Violation Severity
81.8×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
9.5×10%
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

837×

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.

25802×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

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.

621×

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).

Refusal History

DateProductViolationsDivision
9/12/2012
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2580MFRHACCP
Chicago District Office (CHI-DO)
9/12/2012
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
2580MFRHACCP
Chicago District Office (CHI-DO)
2/10/2005
16AET45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/10/2005
16AET45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/10/2005
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
11/17/2004
16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
83NO PROCESS
Seattle District Office (SEA-DO)
8/30/2004
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/30/2004
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/30/2004
16AET45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/11/2002
16CEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.), CAKES, BALLS, ETC.
249FILTHY
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Ottogi SF Corporation's FDA import refusal history?

Ottogi SF Corporation (FEI: 2000003327) has 10 FDA import refusal record(s) in our database, spanning from 3/11/2002 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 SF Corporation's FEI number is 2000003327.

What types of violations has Ottogi SF Corporation received?

Ottogi SF Corporation 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 Ottogi SF Corporation come from?

All FDA import refusal data for Ottogi SF Corporation 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.