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Kikkoman

⚠️ Moderate Risk

FEI: 3007152271 • Minato, Tokyo • JAPAN

FEI

FEI Number

3007152271

📍

Location

Minato, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

Kikkoman (Kabu), 2 Chome 1-1; Nishishinbashi, Minato, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

42.6
LowModerateHighCritical

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

Statistics

8
Total Refusals
3
Unique Violations
9/17/2008
Latest Refusal
10/31/2002
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
13.6×10%
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

838×

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.

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).

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
9/17/2008
29AHE99NONCARBONATED SOFT DRINK, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/17/2008
29AHE99NONCARBONATED SOFT DRINK, N.E.C.
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
11/17/2007
25PGT04MUSHROOM, SHIITAKE , WHOLE (BUTTON) (FUNGI)
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
6/20/2003
38NCE99CONCENTRATED BROTH, N.E.C.
83NO PROCESS
Baltimore District Office (BLT-DO)
11/25/2002
37JCP07STEAK AND OTHER MEAT SAUCE
482NUTRIT LBL
83NO PROCESS
Los Angeles District Office (LOS-DO)
10/31/2002
37JCE07STEAK AND OTHER MEAT SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
10/31/2002
37JCE07STEAK AND OTHER MEAT SAUCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
10/31/2002
38NCE99CONCENTRATED BROTH, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Kikkoman's FDA import refusal history?

Kikkoman (FEI: 3007152271) has 8 FDA import refusal record(s) in our database, spanning from 10/31/2002 to 9/17/2008.

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. Kikkoman's FEI number is 3007152271.

What types of violations has Kikkoman received?

Kikkoman 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 Kikkoman come from?

All FDA import refusal data for Kikkoman 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.