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Kio Yamato Europe

✅ Low Risk

FEI: 3007500385 • Berlin • GERMANY

FEI

FEI Number

3007500385

📍

Location

Berlin

🇩🇪

Country

GERMANY
🏢

Address

4 6 Heinersdorfer, , Berlin, , Germany

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
12/30/2011
Latest Refusal
12/30/2011
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

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).

Refusal History

DateProductViolationsDivision
12/30/2011
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Kio Yamato Europe's FDA import refusal history?

Kio Yamato Europe (FEI: 3007500385) has 1 FDA import refusal record(s) in our database, spanning from 12/30/2011 to 12/30/2011.

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. Kio Yamato Europe's FEI number is 3007500385.

What types of violations has Kio Yamato Europe received?

Kio Yamato Europe 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 Kio Yamato Europe come from?

All FDA import refusal data for Kio Yamato Europe 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.