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Wakodo

⚠️ Moderate Risk

FEI: 1000453765 • Chiyoda, Tokyo • JAPAN

FEI

FEI Number

1000453765

📍

Location

Chiyoda, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

420, Kandasakuma-Cho, Chiyoda, Tokyo, Japan

Moderate Risk

FDA Import Risk Assessment

41.0
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
10/27/2003
Latest Refusal
3/14/2003
Earliest Refusal

Score Breakdown

Violation Severity
68.3×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

833×

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.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

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.

621×

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
10/27/2003
40CET01MILK BASE FORMULA PRODUCT (BABY)
260FALSE
482NUTRIT LBL
Los Angeles District Office (LOS-DO)
3/14/2003
02DHT99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/14/2003
02DHT99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/14/2003
02DHT99RICE, PROCESSED (PACKAGED) N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
3/14/2003
02DGT99RICE, PROCESSED (PACKAGED) N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Wakodo's FDA import refusal history?

Wakodo (FEI: 1000453765) has 5 FDA import refusal record(s) in our database, spanning from 3/14/2003 to 10/27/2003.

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. Wakodo's FEI number is 1000453765.

What types of violations has Wakodo received?

Wakodo has been cited for 4 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 Wakodo come from?

All FDA import refusal data for Wakodo 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.