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Kamada Soy Sauce, Inc.

⚠️ Moderate Risk

FEI: 3004278666 • Sakaide, Kagawa • JAPAN

FEI

FEI Number

3004278666

📍

Location

Sakaide, Kagawa

🇯🇵

Country

JAPAN
🏢

Address

1 Chome 6-35, Hon-Machi, Sakaide, Kagawa, Japan

Moderate Risk

FDA Import Risk Assessment

40.0
LowModerateHighCritical

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

Statistics

9
Total Refusals
6
Unique Violations
8/17/2004
Latest Refusal
8/17/2004
Earliest Refusal

Score Breakdown

Violation Severity
49.6×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

3217×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3247×

NO ENGLISH

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)).

625×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

835×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

2182×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2761×

PRESRV LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.

Refusal History

DateProductViolationsDivision
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
321LACKS N/C
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
321LACKS N/C
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
321LACKS N/C
324NO ENGLISH
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
321LACKS N/C
324NO ENGLISH
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
321LACKS N/C
324NO ENGLISH
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
218LIST INGRE
321LACKS N/C
324NO ENGLISH
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
218LIST INGRE
276PRESRV LBL
321LACKS N/C
New York District Office (NYK-DO)
8/17/2004
28LVF99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Kamada Soy Sauce, Inc.'s FDA import refusal history?

Kamada Soy Sauce, Inc. (FEI: 3004278666) has 9 FDA import refusal record(s) in our database, spanning from 8/17/2004 to 8/17/2004.

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. Kamada Soy Sauce, Inc.'s FEI number is 3004278666.

What types of violations has Kamada Soy Sauce, Inc. received?

Kamada Soy Sauce, Inc. has been cited for 6 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 Kamada Soy Sauce, Inc. come from?

All FDA import refusal data for Kamada Soy Sauce, Inc. 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.