Eduardo Antonio Tavarez
✅ Low Risk
FEI: 1000310485 • D.R. • DOMINICAN REPUBLIC
FEI Number
1000310485
Location
D.R.
Country
DOMINICAN REPUBLICAddress
Villa Linda, No 59-A, , Bonao, D.R., , Dominican Republic
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/6/2004 | 28AGC15CORIANDER, WHOLE (SPICE) | 473LABELING | San Juan District Office (SJN-DO) |
Frequently Asked Questions
What is Eduardo Antonio Tavarez's FDA import refusal history?
Eduardo Antonio Tavarez (FEI: 1000310485) has 1 FDA import refusal record(s) in our database, spanning from 7/6/2004 to 7/6/2004.
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. Eduardo Antonio Tavarez's FEI number is 1000310485.
What types of violations has Eduardo Antonio Tavarez received?
Eduardo Antonio Tavarez 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 Eduardo Antonio Tavarez come from?
All FDA import refusal data for Eduardo Antonio Tavarez 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.