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Allimax International Limited

⚠️ Moderate Risk

FEI: 3004350020 • Rye, East Sussex • UNITED KINGDOM

FEI

FEI Number

3004350020

📍

Location

Rye, East Sussex

🇬🇧
🏢

Address

Playden House Military Road, Military Road, Rye, East Sussex, United Kingdom

Moderate Risk

FDA Import Risk Assessment

45.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

11
Total Refusals
4
Unique Violations
6/13/2023
Latest Refusal
3/18/2003
Earliest Refusal

Score Breakdown

Violation Severity
66.2×40%
Refusal Volume
40.0×30%
Recency
34.2×20%
Frequency
5.4×10%
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

756×

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).

3283×

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.

162×

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.

2562×

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

DateProductViolationsDivision
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)
256INCONSPICU
328USUAL NAME
New Orleans District Office (NOL-DO)
6/3/2005
54FBJ10GARLIC (HERBAL & BOTANICALS, NOT TEAS)
256INCONSPICU
328USUAL NAME
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.