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MISHIMA SHOKUHIN

⚠️ Moderate Risk

FEI: 3010157441 • Hiroshima, Hiroshima • JAPAN

FEI

FEI Number

3010157441

📍

Location

Hiroshima, Hiroshima

🇯🇵

Country

JAPAN
🏢

Address

Mishimashokuhin ( Kabu ), 2 Chome 1-53; Minamiyoshijima; Naka, Hiroshima, Hiroshima, Japan

Moderate Risk

FDA Import Risk Assessment

34.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
7/8/2004
Latest Refusal
8/13/2002
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
10.5×10%
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

2181×

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.

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.

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
7/8/2004
24TGT29SEAWEED (LEAF & STEM VEGETABLE)
218LIST INGRE
238UNSAFE ADD
San Francisco District Office (SAN-DO)
8/13/2002
25PEE99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is MISHIMA SHOKUHIN's FDA import refusal history?

MISHIMA SHOKUHIN (FEI: 3010157441) has 2 FDA import refusal record(s) in our database, spanning from 8/13/2002 to 7/8/2004.

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. MISHIMA SHOKUHIN's FEI number is 3010157441.

What types of violations has MISHIMA SHOKUHIN received?

MISHIMA SHOKUHIN has been cited for 3 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 MISHIMA SHOKUHIN come from?

All FDA import refusal data for MISHIMA SHOKUHIN 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.