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Nichiro K.K.

⚠️ High Risk

FEI: 3001105083 • Chiyoda Ku, Tokyo • JAPAN

FEI

FEI Number

3001105083

📍

Location

Chiyoda Ku, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

Yurakucho, , Chiyoda Ku, Tokyo, Japan

High Risk

FDA Import Risk Assessment

51.5
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

14
Total Refusals
2
Unique Violations
4/30/2003
Latest Refusal
9/4/2002
Earliest Refusal

Score Breakdown

Violation Severity
71.1×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

8314×

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.

2184×

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.

Refusal History

DateProductViolationsDivision
4/30/2003
02DGN99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
02DGN99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
02DGN99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
02DGN99RICE, PROCESSED (PACKAGED) N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
02DGN99RICE, PROCESSED (PACKAGED) N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/30/2003
02DGN99RICE, PROCESSED (PACKAGED) N.E.C.
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/12/2003
02DGT99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
2/12/2003
02DGT99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
218LIST INGRE
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/4/2002
02DGT03RICE, ENRICHED PROCESSED (PACKAGED)
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Nichiro K.K.'s FDA import refusal history?

Nichiro K.K. (FEI: 3001105083) has 14 FDA import refusal record(s) in our database, spanning from 9/4/2002 to 4/30/2003.

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. Nichiro K.K.'s FEI number is 3001105083.

What types of violations has Nichiro K.K. received?

Nichiro K.K. 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 Nichiro K.K. come from?

All FDA import refusal data for Nichiro 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.