KNF Korea Inc
⚠️ Moderate Risk
FEI: 3012622251 • Gangseo-gu, Busangwangyeog-si • SOUTH KOREA
FEI Number
3012622251
Location
Gangseo-gu, Busangwangyeog-si
Country
SOUTH KOREAAddress
83 Pyeonggangro229beon-Gil, , Gangseo-gu, Busangwangyeog-si, 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
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.
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.
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)).
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
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 |
|---|---|---|---|
| 2/28/2019 | 22KGT99OTHER FRUITS AND FRUIT PRODUCTS, OTHER FRUIT JUICES OR CONCENTRATES, N.E.C. | Division of Northeast Imports (DNEI) | |
| 3/7/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/7/2018 | 25MEI31GINSENG, JUICE OR DRINK (ROOT & TUBER VEGETABLE) | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | 324NO ENGLISH | Division of West Coast Imports (DWCI) |
| 3/6/2018 | 25MEI21GARLIC BULB, JUICE OR DRINK | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 22KEI01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 29YEI99SOFT DRINKS AND WATERS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) | |
| 3/6/2018 | 25YEI99VEGETABLE & VEGETABLE PRODUCTS NOT MENTIONED ELSEWHERE, N.E.C. | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is KNF Korea Inc's FDA import refusal history?
KNF Korea Inc (FEI: 3012622251) has 13 FDA import refusal record(s) in our database, spanning from 3/6/2018 to 2/28/2019.
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. KNF Korea Inc's FEI number is 3012622251.
What types of violations has KNF Korea Inc received?
KNF Korea Inc 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 KNF Korea Inc come from?
All FDA import refusal data for KNF Korea Inc 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.