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KAMEDA SEIKA CO.,LTD. SHIRONE PLANT

⚠️ Moderate Risk

FEI: 3004309384 • Niigata-shi, Niigata-ken • JAPAN

FEI

FEI Number

3004309384

📍

Location

Niigata-shi, Niigata-ken

🇯🇵

Country

JAPAN
🏢

Address

481-2, OHAZA SHIRONE, , Niigata-shi, Niigata-ken, Japan

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/3/2008
Latest Refusal
11/3/2008
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

111×

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).

Refusal History

DateProductViolationsDivision
11/3/2008
03FGT07RICE CRACKERS
11UNSAFE COL
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is KAMEDA SEIKA CO.,LTD. SHIRONE PLANT's FDA import refusal history?

KAMEDA SEIKA CO.,LTD. SHIRONE PLANT (FEI: 3004309384) has 1 FDA import refusal record(s) in our database, spanning from 11/3/2008 to 11/3/2008.

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. KAMEDA SEIKA CO.,LTD. SHIRONE PLANT's FEI number is 3004309384.

What types of violations has KAMEDA SEIKA CO.,LTD. SHIRONE PLANT received?

KAMEDA SEIKA CO.,LTD. SHIRONE PLANT 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 KAMEDA SEIKA CO.,LTD. SHIRONE PLANT come from?

All FDA import refusal data for KAMEDA SEIKA CO.,LTD. SHIRONE PLANT 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.