Toko K.K.
⚠️ Moderate Risk
FEI: 3002652050 • Tokyo • JAPAN
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/13/2007 | 24TCT03BAMBOO SHOOTS (LEAF & STEM VEGETABLE) | San Francisco District Office (SAN-DO) | |
| 2/12/2003 | 37JCT99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 2/12/2003 | 37JCT99SAUCES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 2/12/2003 | 25ECT99MIXED VEGETABLES, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 2/11/2003 | 25HCT99MIXED VEGETABLES, WITH SAUCE, N.E.C. | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Toko K.K.'s FDA import refusal history?
Toko K.K. (FEI: 3002652050) has 5 FDA import refusal record(s) in our database, spanning from 2/11/2003 to 3/13/2007.
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. Toko K.K.'s FEI number is 3002652050.
What types of violations has Toko K.K. received?
Toko 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 Toko K.K. come from?
All FDA import refusal data for Toko 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.