SupplierRadar

Mizkan Euro Ltd.

FDA import alert and refusal historyBury St. Edmunds, United KingdomFEI 3004303725

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Mizkan Euro Ltd..

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectMizkan Euro Ltd added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Mizkan Euro Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between November 13, 2017 and July 13, 2020, most often for no scheduled process filed (NO PROCESS).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Red beet (root & tuber vegetable) · NEEDS FCE
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Mizkan Euro Ltd.

7 records, newest first. Each line links to the FDA page it came from.

2023

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2020

  1. Import refusal
    Refused, Red beet (root & tuber vegetable)NEEDS FCENO PROCESSEntry 101-6511773-0
    Source

2018

  1. Import refusal
    Refused, Tzahp choy (chinese canned sweet pickles made from mixed vegetables), with sauceLABELINGEntry KM6-3513180-8
    Source

2017

  1. Import refusal
    Refused, 2 lines in one entry: Tzahp choy (chinese canned sweet pickles made from mixed vegetables), with sauce; Onion bulb (yellow, white, red, etc.) (root & tuber vegetable)PRESRV LBLNO PROCESSEntry BUQ-0139065-9Show 2 lines
    • Refused, Tzahp choy (chinese canned sweet pickles made from mixed vegetables), with saucePRESRV LBLNO PROCESSEntry BUQ-0139065-9Source
    • Refused, Onion bulb (yellow, white, red, etc.) (root & tuber vegetable)NO PROCESSEntry BUQ-0139065-9Source
    Source

2016

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2010

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • NO PROCESS3 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • NEEDS FCE1 refused line

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • PRESRV LBL1 refused line

    Chemical preservative not declared

    The product appeared to contain a chemical preservative without labeling that states that fact and the preservative's function.

Questions about Mizkan Euro Ltd.

Is Mizkan Euro Ltd. on an FDA import alert?
No listing for Mizkan Euro Ltd. 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 Mizkan Euro Ltd.?
Yes. FDA refused 4 shipment lines from Mizkan Euro Ltd. between November 13, 2017 and July 13, 2020. The most recent, on July 13, 2020, was red beet (root & tuber vegetable), charged as NEEDS FCE (processor not registered for canned or acidified foods).
Why did FDA refuse Mizkan Euro Ltd.'s shipments?
The most frequent charges are NO PROCESS (no scheduled process filed, 3 lines) and LABELING (fair packaging and labeling act, 1 line).
When was Mizkan Euro Ltd. last inspected by FDA?
FDA's most recent inspection of Mizkan Euro Ltd. with a final classification is dated March 9, 2023 and was classified NAI (No Action Indicated).
What is Mizkan Euro Ltd.'s FEI number?
Mizkan Euro Ltd.'s FDA Establishment Identifier (FEI) is 3004303725.

Buying from Mizkan Euro Ltd.?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Mizkan Euro Ltd..

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectMizkan Euro Ltd added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.