Unknown
⚠️ High Risk
FEI: 3011198526 • Unknown • CHINA
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
TPLKUSSLLB
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.
TPLACKFIRM
This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
LACKS FIRM
The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
LACKS N/C
The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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.
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
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.
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.
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)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/13/2025 | 07QGT13CORN PUFFS (FLAVORED OR UNFLAVORED), VEGETABLE SNACKS (OTHER THAN PULSES) BAKED | Division of Northeast Imports (DNEI) | |
| 6/7/2024 | 74OMHPERICARDIAL PATCH TO FACILITATE REVISION SURGERIES | Division of Southeast Imports (DSEI) | |
| 9/19/2023 | 61HBA99ANTI-BACTERIAL, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/19/2020 | 62HBK05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/19/2020 | 65FBY02WATER, PURIFIED, U.S.P. (PHARMACEUTIC AID) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/19/2020 | 62HBK05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/19/2020 | 62HBK05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/19/2020 | 62HBK05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/19/2020 | 62HBK05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/28/2020 | 98LCA01E-CIGARETTE | Division of Northeast Imports (DNEI) | |
| 8/14/2020 | 62HAL05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of West Coast Imports (DWCI) |
| 8/14/2020 | 62HAL05ETHYL ALCOHOL (ANTI-MICROBIAL) | 75UNAPPROVED | Division of West Coast Imports (DWCI) |
| 5/16/2019 | 95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL | 47NON STD | Division of Northeast Imports (DNEI) |
| 2/27/2019 | 53HD05NAIL POLISH AND ENAMEL (MANICURING PREPARATIONS) | Division of Northern Border Imports (DNBI) | |
| 2/27/2019 | 53HD05NAIL POLISH AND ENAMEL (MANICURING PREPARATIONS) | Division of Northern Border Imports (DNBI) | |
| 2/27/2019 | 53HD05NAIL POLISH AND ENAMEL (MANICURING PREPARATIONS) | Division of Northern Border Imports (DNBI) | |
| 9/27/2018 | 76EFWTOOTHBRUSH, MANUAL | Division of Southeast Imports (DSEI) | |
| 2/28/2018 | 60LBJ99ANALGESIC, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/28/2018 | 60LBJ99ANALGESIC, N.E.C. | Division of Northeast Imports (DNEI) | |
| 2/28/2018 | 60LBJ99ANALGESIC, N.E.C. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 2/28/2018 | 60LBJ99ANALGESIC, N.E.C. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Unknown's FDA import refusal history?
Unknown (FEI: 3011198526) has 34 FDA import refusal record(s) in our database, spanning from 2/28/2018 to 1/13/2025.
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. Unknown's FEI number is 3011198526.
What types of violations has Unknown received?
Unknown has been cited for 18 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 Unknown come from?
All FDA import refusal data for Unknown 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.