Allimax International Limited
⚠️ Moderate Risk
FEI: 3004350020 • Rye, East Sussex • UNITED KINGDOM
FEI Number
3004350020
Location
Rye, East Sussex
Country
UNITED KINGDOMAddress
Playden House Military Road, Military Road, Rye, East Sussex, United Kingdom
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
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).
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.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
INCONSPICU
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 |
|---|---|---|---|
| 6/13/2023 | 54ABY99VITAMIN, N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 3/24/2022 | 54FCE10GARLIC (HERBAL & BOTANICALS, NOT TEAS) | 75UNAPPROVED | Division of Northern Border Imports (DNBI) |
| 3/24/2022 | 54FCE10GARLIC (HERBAL & BOTANICALS, NOT TEAS) | 75UNAPPROVED | Division of Northern Border Imports (DNBI) |
| 2/11/2014 | 54FCK99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 3/30/2012 | 54YCL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 2/7/2007 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | 16DIRECTIONS | New Orleans District Office (NOL-DO) |
| 2/7/2007 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | 16DIRECTIONS | New Orleans District Office (NOL-DO) |
| 6/3/2005 | 54FCB10GARLIC (HERBAL & BOTANICALS, NOT TEAS) | 328USUAL NAME | New Orleans District Office (NOL-DO) |
| 6/3/2005 | 54FBL10GARLIC (HERBAL & BOTANICALS, NOT TEAS) | New Orleans District Office (NOL-DO) | |
| 6/3/2005 | 54FBJ10GARLIC (HERBAL & BOTANICALS, NOT TEAS) | New Orleans District Office (NOL-DO) | |
| 3/18/2003 | 66VAB99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Allimax International Limited's FDA import refusal history?
Allimax International Limited (FEI: 3004350020) has 11 FDA import refusal record(s) in our database, spanning from 3/18/2003 to 6/13/2023.
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. Allimax International Limited's FEI number is 3004350020.
What types of violations has Allimax International Limited received?
Allimax International Limited has been cited for 4 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 Allimax International Limited come from?
All FDA import refusal data for Allimax International Limited 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.