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Yamasan Shokuhin Co. Ltd.

⚠️ Moderate Risk

FEI: 3004289215 • Nerima, Tokyo • JAPAN

FEI

FEI Number

3004289215

📍

Location

Nerima, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

2 Chome 6-15, Yahara, Nerima, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

49.4
LowModerateHighCritical

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

Statistics

10
Total Refusals
5
Unique Violations
11/5/2015
Latest Refusal
12/9/2014
Earliest Refusal

Score Breakdown

Violation Severity
69.5×40%
Refusal Volume
38.6×30%
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

1110×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2745×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

2383×

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.

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.

4822×

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.

Refusal History

DateProductViolationsDivision
11/5/2015
25JGT26CHINESE RADISH (DAIKON) (ROOT & TUBER VEGETABLE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
6/26/2015
25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
6/26/2015
25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
6/26/2015
25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
6/26/2015
25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
Los Angeles District Office (LOS-DO)
2/3/2015
25JGT26CHINESE RADISH (DAIKON) (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
Los Angeles District Office (LOS-DO)
2/3/2015
25JGP27WHITE RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
Los Angeles District Office (LOS-DO)
2/3/2015
25JGT26CHINESE RADISH (DAIKON) (ROOT & TUBER VEGETABLE)
11UNSAFE COL
238UNSAFE ADD
274COLOR LBLG
Los Angeles District Office (LOS-DO)
12/9/2014
25JGT26CHINESE RADISH (DAIKON) (ROOT & TUBER VEGETABLE)
11UNSAFE COL
218LIST INGRE
238UNSAFE ADD
274COLOR LBLG
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
12/9/2014
25JGT26CHINESE RADISH (DAIKON) (ROOT & TUBER VEGETABLE)
11UNSAFE COL
218LIST INGRE
238UNSAFE ADD
274COLOR LBLG
482NUTRIT LBL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

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

Yamasan Shokuhin Co. Ltd. (FEI: 3004289215) has 10 FDA import refusal record(s) in our database, spanning from 12/9/2014 to 11/5/2015.

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. Yamasan Shokuhin Co. Ltd.'s FEI number is 3004289215.

What types of violations has Yamasan Shokuhin Co. Ltd. received?

Yamasan Shokuhin Co. Ltd. has been cited for 5 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 Yamasan Shokuhin Co. Ltd. come from?

All FDA import refusal data for Yamasan 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.