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Marumiya Shokuhin Kogyo K.K.

⚠️ Moderate Risk

FEI: 1000173523 • Suginami, Tokyo • JAPAN

FEI

FEI Number

1000173523

📍

Location

Suginami, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

1 Chome 15-18, Shoan, Suginami, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

40.8
LowModerateHighCritical

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

Statistics

13
Total Refusals
3
Unique Violations
3/20/2006
Latest Refusal
9/9/2002
Earliest Refusal

Score Breakdown

Violation Severity
61.0×40%
Refusal Volume
42.5×30%
Recency
0.0×20%
Frequency
36.8×10%
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

8310×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

2187×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
3/20/2006
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
218LIST INGRE
Los Angeles District Office (LOS-DO)
4/30/2003
25EGT99MIXED VEGETABLES, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
25EGN99MIXED VEGETABLES, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
25EGT99MIXED VEGETABLES, N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
25EGT99MIXED VEGETABLES, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
25EGT99MIXED VEGETABLES, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/12/2003
27YGT99CONDIMENTS, N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/12/2003
37JGT99SAUCES, N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/12/2003
24VDT99LEAF & STEM VEGETABLES, WITH SAUCE, N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/12/2003
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
218LIST INGRE
Los Angeles District Office (LOS-DO)
2/12/2003
28KGT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
218LIST INGRE
Los Angeles District Office (LOS-DO)
9/9/2002
28LVT99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
473LABELING
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/9/2002
28LVT99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
473LABELING
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Marumiya Shokuhin Kogyo K.K.'s FDA import refusal history?

Marumiya Shokuhin Kogyo K.K. (FEI: 1000173523) has 13 FDA import refusal record(s) in our database, spanning from 9/9/2002 to 3/20/2006.

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 Kogyo K.K.'s FEI number is 1000173523.

What types of violations has Marumiya Shokuhin Kogyo K.K. received?

Marumiya Shokuhin Kogyo K.K. has been cited for 3 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 Kogyo K.K. come from?

All FDA import refusal data for Marumiya Shokuhin Kogyo K.K. 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.