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Myojyo Shokuhin Co., Ltd

⚠️ High Risk

FEI: 1000161852 • Shibuya-Ku, Tokyo • JAPAN

FEI

FEI Number

1000161852

📍

Location

Shibuya-Ku, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

50-11 3-Chome, Sendagaya, , Shibuya-Ku, Tokyo, Japan

High Risk

FDA Import Risk Assessment

52.7
LowModerateHighCritical

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

Statistics

16
Total Refusals
4
Unique Violations
9/10/2002
Latest Refusal
5/10/2002
Earliest Refusal

Score Breakdown

Violation Severity
72.6×40%
Refusal Volume
45.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

8315×

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.

3242×

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)).

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

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).

Refusal History

DateProductViolationsDivision
9/10/2002
04CFT07NOODLES, INSTANT
324NO ENGLISH
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/10/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/9/2002
04CFT07NOODLES, INSTANT
324NO ENGLISH
482NUTRIT LBL
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/9/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/9/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/9/2002
04CFT07NOODLES, INSTANT
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/10/2002
04CGT07NOODLES, INSTANT
62NEEDS FCE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Myojyo Shokuhin Co., Ltd's FDA import refusal history?

Myojyo Shokuhin Co., Ltd (FEI: 1000161852) has 16 FDA import refusal record(s) in our database, spanning from 5/10/2002 to 9/10/2002.

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. Myojyo Shokuhin Co., Ltd's FEI number is 1000161852.

What types of violations has Myojyo Shokuhin Co., Ltd received?

Myojyo Shokuhin 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 Myojyo Shokuhin Co., Ltd come from?

All FDA import refusal data for Myojyo Shokuhin 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.