DIMTA
⚠️ Moderate Risk
FEI: 3012553712 • San To Domingo • DOMINICAN REPUBLIC
FEI Number
3012553712
Location
San To Domingo
Country
DOMINICAN REPUBLICAddress
Manuela Diez 240 Villa, , San To 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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/22/2016 | 53DD02PERFUMES (FRAGRANCE PREPARATIONS) | 473LABELING | San Juan District Office (SJN-DO) |
| 11/22/2016 | 53ED05RINSES (HAIR PREPARATIONS, NON-COLORING) | 473LABELING | San Juan District Office (SJN-DO) |
| 11/22/2016 | 53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 473LABELING | San Juan District Office (SJN-DO) |
| 11/22/2016 | 53CC99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | 473LABELING | San Juan District Office (SJN-DO) |
| 11/22/2016 | 53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 473LABELING | Division of Southeast Imports (DSEI) |
| 11/22/2016 | 53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 473LABELING | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is DIMTA's FDA import refusal history?
DIMTA (FEI: 3012553712) has 6 FDA import refusal record(s) in our database, spanning from 11/22/2016 to 11/22/2016.
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. DIMTA's FEI number is 3012553712.
What types of violations has DIMTA received?
DIMTA 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 DIMTA come from?
All FDA import refusal data for DIMTA 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.