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KOHYO CO., LTD.

⚠️ Moderate Risk

FEI: 3004324486 • Yokkaichi, MIE • JAPAN

FEI

FEI Number

3004324486

📍

Location

Yokkaichi, MIE

🇯🇵

Country

JAPAN
🏢

Address

5 Chome 4-19, Shinsho, Yokkaichi, MIE, Japan

Moderate Risk

FDA Import Risk Assessment

30.0
LowModerateHighCritical

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

Statistics

9
Total Refusals
4
Unique Violations
12/27/2019
Latest Refusal
2/11/2003
Earliest Refusal

Score Breakdown

Violation Severity
46.0×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
5.3×10%
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

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)).

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

621×

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).

831×

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.

Refusal History

DateProductViolationsDivision
12/27/2019
29BGE99CARBONATED SOFT DRINK, N.E.C.
324NO ENGLISH
Division of Southeast Imports (DSEI)
12/27/2019
29BGE99CARBONATED SOFT DRINK, N.E.C.
324NO ENGLISH
Division of Southeast Imports (DSEI)
12/27/2019
29BGE99CARBONATED SOFT DRINK, N.E.C.
324NO ENGLISH
Division of Southeast Imports (DSEI)
12/27/2019
29BGE99CARBONATED SOFT DRINK, N.E.C.
324NO ENGLISH
Division of Southeast Imports (DSEI)
12/27/2019
25FGE13KIMCHI, DRIED OR PASTE
324NO ENGLISH
Division of Southeast Imports (DSEI)
12/27/2019
07QGE08SEAWEED SNACKS (FLAVORED OR UNFLAVORED), VEGETABLE SNACKS (OTHER THAN PULSES) BAKED
324NO ENGLISH
Division of Southeast Imports (DSEI)
12/27/2019
16AGE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
324NO ENGLISH
Division of Southeast Imports (DSEI)
10/29/2003
37JGT99SAUCES, N.E.C.
62NEEDS FCE
83NO PROCESS
Florida District Office (FLA-DO)
2/11/2003
16AGH36SMELT
308MFR INSAN
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is KOHYO CO., LTD.'s FDA import refusal history?

KOHYO CO., LTD. (FEI: 3004324486) has 9 FDA import refusal record(s) in our database, spanning from 2/11/2003 to 12/27/2019.

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. KOHYO CO., LTD.'s FEI number is 3004324486.

What types of violations has KOHYO CO., LTD. received?

KOHYO CO., LTD. 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 KOHYO CO., LTD. come from?

All FDA import refusal data for KOHYO CO., LTD. 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.