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Kaiko

⚠️ Moderate Risk

FEI: 3009493127 • Kagoshima, Kagoshima • JAPAN

FEI

FEI Number

3009493127

📍

Location

Kagoshima, Kagoshima

🇯🇵

Country

JAPAN
🏢

Address

2 Chome 2-20, Taniyamako, Kagoshima, Kagoshima, Japan

Moderate Risk

FDA Import Risk Assessment

47.2
LowModerateHighCritical

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

Statistics

5
Total Refusals
1
Unique Violations
9/22/2016
Latest Refusal
10/20/2014
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
26.0×10%
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

3085×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
9/22/2016
16AGT01ANCHOVY
308MFR INSAN
Los Angeles District Office (LOS-DO)
9/22/2016
16AGT01ANCHOVY
308MFR INSAN
Los Angeles District Office (LOS-DO)
9/22/2016
16AGT01ANCHOVY
308MFR INSAN
Los Angeles District Office (LOS-DO)
4/22/2015
16AGT01ANCHOVY
308MFR INSAN
Los Angeles District Office (LOS-DO)
10/20/2014
16AGH01ANCHOVY
308MFR INSAN
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Kaiko's FDA import refusal history?

Kaiko (FEI: 3009493127) has 5 FDA import refusal record(s) in our database, spanning from 10/20/2014 to 9/22/2016.

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. Kaiko's FEI number is 3009493127.

What types of violations has Kaiko received?

Kaiko 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 Kaiko come from?

All FDA import refusal data for Kaiko 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.