SupplierRadar

Tokai Kanzume Co., Ltd. Kameyama Factory

FDA import alert and refusal historyKamie, JapanFEI 3012521509

Recorded by FDA as TOKAI KANZUME CO., LTD. KAMEYAMA FACTORY

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Tokai Kanzume Co., Ltd. Kameyama Factory.

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

Example subjectTokai Kanzume Co., Ltd. Kameyama Factor added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Tokai Kanzume Co., Ltd. Kameyama Factory is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on April 20, 2021, most often for net quantity statement missing (LACKS N/C).

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

Current status

Import alerts
Not listed
Last import refusal
Miso (soybean base) broth (meat and/or vegetable stock) · LACKS N/C
Last warning letter
None found
Last inspection
None on record

Every FDA record for Tokai Kanzume Co., Ltd. Kameyama Factory

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

2021

  1. Import refusal
    Refused, 2 lines in one entry: Miso (soybean base) broth (meat and/or vegetable stock)LACKS N/CNO ENGLISHUSUAL NAMENUTRIT LBLEntry 9ES-0057330-1Show 2 lines
    Source

Refusal charges, in plain English

  • LACKS N/C2 refused lines

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • NO ENGLISH2 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • NO PROCESS2 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.

  • NUTRIT LBL2 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • USUAL NAME2 refused lines

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

Questions about Tokai Kanzume Co., Ltd. Kameyama Factory

Is Tokai Kanzume Co., Ltd. Kameyama Factory on an FDA import alert?
No listing for Tokai Kanzume Co., Ltd. Kameyama Factory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
Has FDA refused shipments from Tokai Kanzume Co., Ltd. Kameyama Factory?
Yes. FDA refused 2 shipment lines from Tokai Kanzume Co., Ltd. Kameyama Factory on April 20, 2021. The most recent, on April 20, 2021, was miso (soybean base) broth (meat and/or vegetable stock), charged as LACKS N/C (net quantity statement missing).
Why did FDA refuse Tokai Kanzume Co., Ltd. Kameyama Factory's shipments?
The most frequent charges are LACKS N/C (net quantity statement missing, 2 lines) and NO ENGLISH (required label information not in english, 2 lines).
What is Tokai Kanzume Co., Ltd. Kameyama Factory's FEI number?
Tokai Kanzume Co., Ltd. Kameyama Factory's FDA Establishment Identifier (FEI) is 3012521509.

Buying from Tokai Kanzume Co., Ltd. Kameyama Factory?

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 Tokai Kanzume Co., Ltd. Kameyama Factory.

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

Example subjectTokai Kanzume Co., Ltd. Kameyama Factor 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.