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MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY

⚠️ Moderate Risk

FEI: 3004263020 • Futaba-Gun, Fukushima • JAPAN

FEI

FEI Number

3004263020

📍

Location

Futaba-Gun, Fukushima

🇯🇵

Country

JAPAN
🏢

Address

1-3, Oazakamikitaba; Hirono-Machi, Futaba-Gun, Fukushima, Japan

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
9/15/2009
Latest Refusal
7/23/2004
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
3.9×10%
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

112×

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).

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

Refusal History

DateProductViolationsDivision
9/15/2009
16YGD04FISH ROE, FISHERY PRODUCTS, N.E.C.
11UNSAFE COL
274COLOR LBLG
New York District Office (NYK-DO)
7/23/2004
16YGT04FISH ROE, FISHERY PRODUCTS, N.E.C.
11UNSAFE COL
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY's FDA import refusal history?

MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY (FEI: 3004263020) has 2 FDA import refusal record(s) in our database, spanning from 7/23/2004 to 9/15/2009.

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. MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY's FEI number is 3004263020.

What types of violations has MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY received?

MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY 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 MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY come from?

All FDA import refusal data for MITSUTOYO CO.,LTD.FUKUSHIMA FACTORY 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.