Indusbello Ind Instru Odont
⚠️ Moderate Risk
FEI: 3008318944 • Londrina, Parana • BRAZIL
FEI Number
3008318944
Location
Londrina, Parana
Country
BRAZILAddress
Rua Tereza de Souza 171, , Londrina, Parana, Brazil
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 Indusbello Ind Instru Odont's FDA import refusal history?
Indusbello Ind Instru Odont (FEI: 3008318944) has 2 FDA import refusal record(s) in our database, spanning from 6/18/2012 to 6/18/2012.
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. Indusbello Ind Instru Odont's FEI number is 3008318944.
What types of violations has Indusbello Ind Instru Odont received?
Indusbello Ind Instru Odont 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 Indusbello Ind Instru Odont come from?
All FDA import refusal data for Indusbello Ind Instru Odont 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.