Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory
⚠️ Moderate Risk
FEI: 3003219499 • Daeduk • SOUTH KOREA
FEI Number
3003219499
Location
Daeduk
Country
SOUTH KOREAAddress
42-1 Moonpyungng, Daejeon, Daeduk, , 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 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).
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).
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)).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
STD IDENT
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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/3/2016 | 29BET99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 1/8/2016 | 29AET09SOFT DRINK, OTHER FRUIT FLAVORED, NONCARBONATED | 62NEEDS FCE | Los Angeles District Office (LOS-DO) |
| 12/8/2015 | 29AET99NONCARBONATED SOFT DRINK, N.E.C. | 62NEEDS FCE | Los Angeles District Office (LOS-DO) |
| 12/8/2015 | 29AET99NONCARBONATED SOFT DRINK, N.E.C. | 62NEEDS FCE | Los Angeles District Office (LOS-DO) |
| 12/8/2015 | 29AET99NONCARBONATED SOFT DRINK, N.E.C. | 62NEEDS FCE | Los Angeles District Office (LOS-DO) |
| 7/8/2015 | 29AEE99NONCARBONATED SOFT DRINK, N.E.C. | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 7/9/2013 | 29AHT03SOFT DRINK, CORE FRUIT FLAVORED, NONCARBONATED | Seattle District Office (SEA-DO) | |
| 7/9/2013 | 29YGT99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Seattle District Office (SEA-DO) | |
| 9/2/2011 | 29AHT01SOFT DRINK, BERRY FRUIT FLAVORED, NONCARBONATED | San Francisco District Office (SAN-DO) | |
| 3/19/2003 | 29BET01SOFT DRINK, BERRY FRUIT FLAVORED, CARBONATED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory's FDA import refusal history?
Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory (FEI: 3003219499) has 10 FDA import refusal record(s) in our database, spanning from 3/19/2003 to 3/3/2016.
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. Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory's FEI number is 3003219499.
What types of violations has Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory received?
Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory has been cited for 9 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 Lotte Chilsung Beverage Co., Ltd. - Daejeon Factory come from?
All FDA import refusal data for Lotte Chilsung Beverage Co., Ltd. - Daejeon 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.