Daerim Co., Ltd.
⚠️ Moderate Risk
FEI: 3002164398 • Seoul • SOUTH KOREA
FEI Number
3002164398
Location
Seoul
Country
SOUTH KOREAAddress
482-2, Bangbae-Dong, Seocho-Gu, , Seoul, , 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
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
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).
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.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/10/2011 | 16AGH01ANCHOVY | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 8/30/2010 | 16AGH01ANCHOVY | 306INSANITARY | Los Angeles District Office (LOS-DO) |
| 3/30/2009 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 3/30/2009 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | Los Angeles District Office (LOS-DO) | |
| 3/30/2009 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | 11UNSAFE COL | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Daerim Co., Ltd.'s FDA import refusal history?
Daerim Co., Ltd. (FEI: 3002164398) has 5 FDA import refusal record(s) in our database, spanning from 3/30/2009 to 6/10/2011.
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. Daerim Co., Ltd.'s FEI number is 3002164398.
What types of violations has Daerim Co., Ltd. received?
Daerim Co., Ltd. has been cited for 6 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 Daerim Co., Ltd. come from?
All FDA import refusal data for Daerim Co., Ltd. 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.