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Nihon Clinic Co Ltd

⚠️ Moderate Risk

FEI: 3006703018 • Kyoto, Kyoto • JAPAN

FEI

FEI Number

3006703018

📍

Location

Kyoto, Kyoto

🇯🇵

Country

JAPAN
🏢

Address

10 Chome 1 Uzumasasanbi-Cho, Ukyo; Shin-Machi; Fushimi, Kyoto, Kyoto, 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
9/18/2008
Latest Refusal
9/18/2008
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

481×

NEEDS ACID

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate acidification.

Refusal History

DateProductViolationsDivision
9/18/2008
54YCL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
48NEEDS ACID
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Nihon Clinic Co Ltd's FDA import refusal history?

Nihon Clinic Co Ltd (FEI: 3006703018) has 1 FDA import refusal record(s) in our database, spanning from 9/18/2008 to 9/18/2008.

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. Nihon Clinic Co Ltd's FEI number is 3006703018.

What types of violations has Nihon Clinic Co Ltd received?

Nihon Clinic 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 Nihon Clinic Co Ltd come from?

All FDA import refusal data for Nihon Clinic 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.