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Kyokuyo Shokuhin Co., Ltd Shiogama Factory

⚠️ High Risk

FEI: 3009863890 • Shiogama, Miyagi • JAPAN

FEI

FEI Number

3009863890

📍

Location

Shiogama, Miyagi

🇯🇵

Country

JAPAN
🏢

Address

3 Chome 20-1, Shinhama-Cho, Shiogama, Miyagi, Japan

High Risk

FDA Import Risk Assessment

56.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

5
Total Refusals
4
Unique Violations
6/12/2025
Latest Refusal
3/28/2013
Earliest Refusal

Score Breakdown

Violation Severity
82.7×40%
Refusal Volume
28.8×30%
Recency
73.9×20%
Frequency
4.1×10%
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

624×

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).

834×

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.

3062×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

Refusal History

DateProductViolationsDivision
6/12/2025
16RGT02CRAB, IMITATION
238UNSAFE ADD
Division of West Coast Imports (DWCI)
5/16/2013
16AET21HERRING
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/16/2013
16AET73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
306INSANITARY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/28/2013
16AEE21HERRING
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/28/2013
16AEE76SAURY
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Kyokuyo Shokuhin Co., Ltd Shiogama Factory's FDA import refusal history?

Kyokuyo Shokuhin Co., Ltd Shiogama Factory (FEI: 3009863890) has 5 FDA import refusal record(s) in our database, spanning from 3/28/2013 to 6/12/2025.

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. Kyokuyo Shokuhin Co., Ltd Shiogama Factory's FEI number is 3009863890.

What types of violations has Kyokuyo Shokuhin Co., Ltd Shiogama Factory received?

Kyokuyo Shokuhin Co., Ltd Shiogama Factory 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 Kyokuyo Shokuhin Co., Ltd Shiogama Factory come from?

All FDA import refusal data for Kyokuyo Shokuhin Co., Ltd Shiogama Factory 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.