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Shimizushi Nokyo., Ihara Plant

⚠️ Moderate Risk

FEI: 1000338608 • Shimizu, Shizuoka • JAPAN

FEI

FEI Number

1000338608

📍

Location

Shimizu, Shizuoka

🇯🇵

Country

JAPAN
🏢

Address

34 1, Ihara-Cho, Shimizu, Shizuoka, Japan

Moderate Risk

FDA Import Risk Assessment

31.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
10/1/2007
Latest Refusal
9/10/2002
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
4.0×10%
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

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

Refusal History

DateProductViolationsDivision
10/1/2007
31AEE99COFFEE, N.E.C.
62NEEDS FCE
San Francisco District Office (SAN-DO)
9/10/2002
29AHT99NONCARBONATED SOFT DRINK, N.E.C.
260FALSE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Shimizushi Nokyo., Ihara Plant's FDA import refusal history?

Shimizushi Nokyo., Ihara Plant (FEI: 1000338608) has 2 FDA import refusal record(s) in our database, spanning from 9/10/2002 to 10/1/2007.

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. Shimizushi Nokyo., Ihara Plant's FEI number is 1000338608.

What types of violations has Shimizushi Nokyo., Ihara Plant received?

Shimizushi Nokyo., Ihara Plant 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 Shimizushi Nokyo., Ihara Plant come from?

All FDA import refusal data for Shimizushi Nokyo., Ihara 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.