IKEDA MOHANDO CO LTD
✅ Low Risk
FEI: 3012836331 • Nakaniikawa-Gun, Toyama • JAPAN
FEI Number
3012836331
Location
Nakaniikawa-Gun, Toyama
Country
JAPANAddress
16, Kanda; Kamiichi-Machi, Nakaniikawa-Gun, Toyama, Japan
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/25/2020 | 61XDL08CHLORPHENIRAMINE MALEATE (ANTI-HISTAMINIC) | 3280FRNMFGREG | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is IKEDA MOHANDO CO LTD's FDA import refusal history?
IKEDA MOHANDO CO LTD (FEI: 3012836331) has 1 FDA import refusal record(s) in our database, spanning from 3/25/2020 to 3/25/2020.
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. IKEDA MOHANDO CO LTD's FEI number is 3012836331.
What types of violations has IKEDA MOHANDO CO LTD received?
IKEDA MOHANDO CO LTD has been cited for 1 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 IKEDA MOHANDO CO LTD come from?
All FDA import refusal data for IKEDA MOHANDO 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.