Allimax International Limited
FDA import alert and refusal historyRye, United KingdomFEI 3004350020
As of October 26, 2026, Allimax International Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between March 24, 2022 and June 13, 2023, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Allimax International Limited
3 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Vitamin, n.e.c.UNAPPROVEDEntry AEK-3204372-9Source
2022
- Import refusalSource
Refused, 2 lines in one entry: Garlic (herbal & botanicals, not teas)UNAPPROVEDEntry E5G-0165881-1Show 2 linesHide lines
- Refused, Garlic (herbal & botanicals, not teas)UNAPPROVEDEntry E5G-0165881-1Source
- Refused, Garlic (herbal & botanicals, not teas)UNAPPROVEDEntry E5G-0165881-1Source
Refusal charges, in plain English
- UNAPPROVED3 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Allimax International Limited
- Is Allimax International Limited on an FDA import alert?
- No listing for Allimax International Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the United Kingdom page.
- Has FDA refused shipments from Allimax International Limited?
- Yes. FDA refused 3 shipment lines from Allimax International Limited between March 24, 2022 and June 13, 2023. The most recent, on June 13, 2023, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Allimax International Limited's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
- What is Allimax International Limited's FEI number?
- Allimax International Limited's FDA Establishment Identifier (FEI) is 3004350020.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.