Good Morning Seoul Corp.
⚠️ Moderate Risk
FEI: 3004060910 • Tongduchon, Kyonggi • SOUTH KOREA
FEI Number
3004060910
Location
Tongduchon, Kyonggi
Country
SOUTH KOREAAddress
Sangbongamdong 147 16, , Tongduchon, Kyonggi, South Korea
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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.
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.
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.
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.
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.
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.
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.
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).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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 | Division of West Coast Imports (DWCI) | |
| 6/15/2018 | 24AGB07KIDNEY BEAN | 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 | 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 | Division of Northeast Imports (DNEI) | |
| 9/3/2014 | 24AGE51PEAS | Division of Northeast Imports (DNEI) | |
| 9/3/2014 | 24AGE07KIDNEY BEAN | Division of Northeast Imports (DNEI) | |
| 6/17/2013 | 24AGE07KIDNEY BEAN | Los Angeles District Office (LOS-DO) | |
| 4/8/2011 | 24BVE99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE) | 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.