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MARUMIYA SHOKUHIN KOUGYO,INC.

⚠️ Moderate Risk

FEI: 3009760730 • Hidaka, Saitama • JAPAN

FEI

FEI Number

3009760730

📍

Location

Hidaka, Saitama

🇯🇵

Country

JAPAN
🏢

Address

935, Oazaasahigaoka, Hidaka, Saitama, Japan

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
6/11/2014
Latest Refusal
6/11/2014
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

623×

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
6/11/2014
25EGT99MIXED VEGETABLES, N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)
6/11/2014
25EGT99MIXED VEGETABLES, N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)
6/11/2014
24AGT19ADZUKI BEANS
62NEEDS FCE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is MARUMIYA SHOKUHIN KOUGYO,INC.'s FDA import refusal history?

MARUMIYA SHOKUHIN KOUGYO,INC. (FEI: 3009760730) has 3 FDA import refusal record(s) in our database, spanning from 6/11/2014 to 6/11/2014.

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. MARUMIYA SHOKUHIN KOUGYO,INC.'s FEI number is 3009760730.

What types of violations has MARUMIYA SHOKUHIN KOUGYO,INC. received?

MARUMIYA SHOKUHIN KOUGYO,INC. 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 MARUMIYA SHOKUHIN KOUGYO,INC. come from?

All FDA import refusal data for MARUMIYA SHOKUHIN KOUGYO,INC. 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.