Daikyo Seiko Ltd
⚠️ Moderate Risk
FEI: 1000170295 • Sumida, Tokyo • JAPAN
FEI Number
1000170295
Location
Sumida, Tokyo
Country
JAPANAddress
3 Chome 38-2, Sumida, Sumida, 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
Frequently Asked Questions
What is Daikyo Seiko Ltd's FDA import refusal history?
Daikyo Seiko Ltd (FEI: 1000170295) has 2 FDA import refusal record(s) in our database, spanning from 10/1/2003 to 7/16/2009.
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. Daikyo Seiko Ltd's FEI number is 1000170295.
What types of violations has Daikyo Seiko Ltd received?
Daikyo Seiko 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 Daikyo Seiko Ltd come from?
All FDA import refusal data for Daikyo Seiko 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.