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Daikatsu Suisan Co., Ltd.

⚠️ Moderate Risk

FEI: 3004134912 • Ibaraki • JAPAN

FEI

FEI Number

3004134912

📍

Location

Ibaraki

🇯🇵

Country

JAPAN
🏢

Address

1237 Isohama-Cho, Oharai-Machi, , Higashi Ibaraki-Gun, Ibaraki, , Japan

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
12/13/2010
Latest Refusal
11/10/2010
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2952×

LISTERIA

The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.

Refusal History

DateProductViolationsDivision
12/13/2010
16AGT73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
295LISTERIA
Los Angeles District Office (LOS-DO)
11/10/2010
16AGT73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
295LISTERIA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Daikatsu Suisan Co., Ltd.'s FDA import refusal history?

Daikatsu Suisan Co., Ltd. (FEI: 3004134912) has 2 FDA import refusal record(s) in our database, spanning from 11/10/2010 to 12/13/2010.

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. Daikatsu Suisan Co., Ltd.'s FEI number is 3004134912.

What types of violations has Daikatsu Suisan Co., Ltd. received?

Daikatsu Suisan Co., Ltd. has been cited for 1 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 Daikatsu Suisan Co., Ltd. come from?

All FDA import refusal data for Daikatsu Suisan 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.