Ines Aguiar
⚠️ Moderate Risk
FEI: 3004051697 • Santo Domingo • DOMINICAN REPUBLIC
FEI Number
3004051697
Location
Santo Domingo
Country
DOMINICAN REPUBLICAddress
Avenida Enriquillo 56, , Santo Domingo, , Dominican Republic
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
COUMARIN
The article appears to bear or contain Coumarin, a poisonous or deleterious substance, which may render it injurious to health.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
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.
Refusal History
Frequently Asked Questions
What is Ines Aguiar's FDA import refusal history?
Ines Aguiar (FEI: 3004051697) has 2 FDA import refusal record(s) in our database, spanning from 12/16/2003 to 4/7/2004.
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. Ines Aguiar's FEI number is 3004051697.
What types of violations has Ines Aguiar received?
Ines Aguiar has been cited for 4 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 Ines Aguiar come from?
All FDA import refusal data for Ines Aguiar 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.