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KATOKICHI CO., LTD.

⚠️ Moderate Risk

FEI: 3005411343 • Kan'Onji, Kagawa • JAPAN

FEI

FEI Number

3005411343

📍

Location

Kan'Onji, Kagawa

🇯🇵

Country

JAPAN
🏢

Address

Sakuda-Machi 582, Kunita-Cho, Kan'Onji, Kagawa, Japan

Moderate Risk

FDA Import Risk Assessment

46.5
LowModerateHighCritical

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

Statistics

5
Total Refusals
3
Unique Violations
3/9/2004
Latest Refusal
12/31/2002
Earliest Refusal

Score Breakdown

Violation Severity
84.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
42.0×10%
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

93×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

2181×

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.

831×

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.

Refusal History

DateProductViolationsDivision
3/9/2004
16JGT01CRAB
9SALMONELLA
Baltimore District Office (BLT-DO)
11/13/2003
16KGT01CRAB, BREADED
9SALMONELLA
Baltimore District Office (BLT-DO)
10/29/2003
04CGT05NOODLES, WHEAT AND SOY
218LIST INGRE
Los Angeles District Office (LOS-DO)
4/28/2003
16JGT01CRAB
9SALMONELLA
Baltimore District Office (BLT-DO)
12/31/2002
04CGD09NOODLES, IMITATION
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is KATOKICHI CO., LTD.'s FDA import refusal history?

KATOKICHI CO., LTD. (FEI: 3005411343) has 5 FDA import refusal record(s) in our database, spanning from 12/31/2002 to 3/9/2004.

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. KATOKICHI CO., LTD.'s FEI number is 3005411343.

What types of violations has KATOKICHI CO., LTD. received?

KATOKICHI CO., LTD. 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 KATOKICHI CO., LTD. come from?

All FDA import refusal data for KATOKICHI CO., LTD. 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.