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Takeuchi Seika Kabushikigaisha

⚠️ Moderate Risk

FEI: 2000013047 • Kaga, Ishikawa • JAPAN

FEI

FEI Number

2000013047

📍

Location

Kaga, Ishikawa

🇯🇵

Country

JAPAN
🏢

Address

Wa 101-1 Daishoji Mitsu-Machi, Isikawa; Daishojimitsu-Machi, Kaga, Ishikawa, Japan

Moderate Risk

FDA Import Risk Assessment

30.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
2/24/2010
Latest Refusal
9/8/2006
Earliest Refusal

Score Breakdown

Violation Severity
56.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
8.7×10%
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

112×

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).

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.

3212×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

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.

Refusal History

DateProductViolationsDivision
2/24/2010
34CGE04CHOCOLATE COVERED CANDY PIECES, WITH NUTS OR NUT PRODUCTS (NOT COCONUT)
218LIST INGRE
3300ALLERGEN
San Francisco District Office (SAN-DO)
12/1/2008
34CGE04CHOCOLATE COVERED CANDY PIECES, WITH NUTS OR NUT PRODUCTS (NOT COCONUT)
11UNSAFE COL
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
San Francisco District Office (SAN-DO)
9/8/2006
03JGF06FRUIT FILLED FILLED/ICED COOKIES,BISCUITS AND WAFERS
11UNSAFE COL
321LACKS N/C
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Takeuchi Seika Kabushikigaisha's FDA import refusal history?

Takeuchi Seika Kabushikigaisha (FEI: 2000013047) has 3 FDA import refusal record(s) in our database, spanning from 9/8/2006 to 2/24/2010.

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. Takeuchi Seika Kabushikigaisha's FEI number is 2000013047.

What types of violations has Takeuchi Seika Kabushikigaisha received?

Takeuchi Seika Kabushikigaisha 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 Takeuchi Seika Kabushikigaisha come from?

All FDA import refusal data for Takeuchi Seika Kabushikigaisha 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.