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KOBAYASHI SEIKO

⚠️ Moderate Risk

FEI: 3013930895 • Chuo, Osaka • JAPAN

FEI

FEI Number

3013930895

📍

Location

Chuo, Osaka

🇯🇵

Country

JAPAN
🏢

Address

4 4-10, Doshomachi, Chuo, Osaka, Japan

Moderate Risk

FDA Import Risk Assessment

36.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
2/28/2024
Latest Refusal
2/28/2024
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
62.7×20%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
2/28/2024
62MAD08MENTHOL (ANTI-PRURITIC)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is KOBAYASHI SEIKO's FDA import refusal history?

KOBAYASHI SEIKO (FEI: 3013930895) has 1 FDA import refusal record(s) in our database, spanning from 2/28/2024 to 2/28/2024.

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. KOBAYASHI SEIKO's FEI number is 3013930895.

What types of violations has KOBAYASHI SEIKO received?

KOBAYASHI SEIKO has been cited for 2 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 KOBAYASHI SEIKO come from?

All FDA import refusal data for KOBAYASHI SEIKO 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.