ImportRefusal LogoImportRefusal

Good Morning Seoul Corp.

⚠️ Moderate Risk

FEI: 3004060910 • Tongduchon, Kyonggi • SOUTH KOREA

FEI

FEI Number

3004060910

📍

Location

Tongduchon, Kyonggi

🇰🇷
🏢

Address

Sangbongamdong 147 16, , Tongduchon, Kyonggi, 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

20
Total Refusals
11
Unique Violations
10/2/2019
Latest Refusal
4/8/2011
Earliest Refusal

Score Breakdown

Violation Severity
70.5×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
23.6×10%
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

486×

NEEDS ACID

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate acidification.

1816×

UNDER PRC

The article appears to have inadequate processing in having been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.

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.

3203×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3213×

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.

3283×

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.

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

3063×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

622×

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).

38412×

AF-NONRSP

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the product appears to have been prepared or packed under insanitary conditions whereby it may have been rendered injurious to health due to inadequate processing in that the scheduled process filed by the manufacturer for this acidified food pursuant to 21 CFR 108.25 (c)(2) appears to be inadequate to protect the public health.

31611×

NONRSP-PRC

The article appears to have been prepared or packed under insanitary conditions whereby it may have been rendered injurious to health due to inadequate processing in that the scheduled process filed by the manufacturer pursuant to 21 CFR 108.35(c)(2) appears to be inadequate to protect the public health.

Refusal History

DateProductViolationsDivision
10/2/2019
23FET04CHESTNUT, TOPPING
48NEEDS ACID
Division of West Coast Imports (DWCI)
10/2/2019
24AET07KIDNEY BEAN
48NEEDS ACID
Division of West Coast Imports (DWCI)
10/2/2019
24AET07KIDNEY BEAN
48NEEDS ACID
Division of West Coast Imports (DWCI)
6/15/2018
24AGB07KIDNEY BEAN
306INSANITARY
48NEEDS ACID
Division of West Coast Imports (DWCI)
6/15/2018
24AGB07KIDNEY BEAN
306INSANITARY
48NEEDS ACID
Division of West Coast Imports (DWCI)
4/3/2017
24BET19ADZUKI BEANS, DRIED OR PASTE
3841AF-NONRSP
Division of West Coast Imports (DWCI)
4/3/2017
23BET04CHESTNUT, SHELLED
3841AF-NONRSP
Division of West Coast Imports (DWCI)
3/8/2016
23BET04CHESTNUT, SHELLED
306INSANITARY
48NEEDS ACID
Los Angeles District Office (LOS-DO)
11/18/2015
24AGE07KIDNEY BEAN
181UNDER PRC
Division of Northeast Imports (DNEI)
11/18/2015
24AGE07KIDNEY BEAN
181UNDER PRC
Division of Northeast Imports (DNEI)
11/18/2015
24AGE51PEAS
181UNDER PRC
Division of Northeast Imports (DNEI)
11/18/2015
24AGE07KIDNEY BEAN
181UNDER PRC
Division of Northeast Imports (DNEI)
11/18/2015
24AGE07KIDNEY BEAN
181UNDER PRC
Division of Northeast Imports (DNEI)
11/18/2015
24AGE07KIDNEY BEAN
181UNDER PRC
Division of Northeast Imports (DNEI)
10/14/2015
24BEI99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE)
3161NONRSP-PRC
Los Angeles District Office (LOS-DO)
9/3/2014
24AGE07KIDNEY BEAN
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
83NO PROCESS
Division of Northeast Imports (DNEI)
9/3/2014
24AGE51PEAS
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
83NO PROCESS
Division of Northeast Imports (DNEI)
9/3/2014
24AGE07KIDNEY BEAN
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
83NO PROCESS
Division of Northeast Imports (DNEI)
6/17/2013
24AGE07KIDNEY BEAN
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/8/2011
24BVE99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE)
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Good Morning Seoul Corp.'s FDA import refusal history?

Good Morning Seoul Corp. (FEI: 3004060910) has 20 FDA import refusal record(s) in our database, spanning from 4/8/2011 to 10/2/2019.

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. Good Morning Seoul Corp.'s FEI number is 3004060910.

What types of violations has Good Morning Seoul Corp. received?

Good Morning Seoul Corp. has been cited for 11 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 Good Morning Seoul Corp. come from?

All FDA import refusal data for Good Morning Seoul Corp. 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.