Flobeman
⚠️ Moderate Risk
FEI: 3011250290 • Santo Domingo Este, DO-01 • DOMINICAN REPUBLIC
FEI Number
3011250290
Location
Santo Domingo Este, DO-01
Country
DOMINICAN REPUBLICAddress
Calle presidente Caamano no.16, Los Frailes III, Santo Domingo Este, DO-01, 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
FSVP VIO
The article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) in that it appears that the importer (as defined in section 805 of the FD&C Act) is in violation of section 805.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/6/2025 | 03FGT99CRACKERS (NON FILLED) N.E.C. | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
| 1/6/2025 | 03FGT99CRACKERS (NON FILLED) N.E.C. | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
| 1/6/2025 | 03FGT99CRACKERS (NON FILLED) N.E.C. | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
| 1/6/2025 | 03FGT99CRACKERS (NON FILLED) N.E.C. | 3886FSVP VIO | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Flobeman's FDA import refusal history?
Flobeman (FEI: 3011250290) has 4 FDA import refusal record(s) in our database, spanning from 1/6/2025 to 1/6/2025.
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. Flobeman's FEI number is 3011250290.
What types of violations has Flobeman received?
Flobeman 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 Flobeman come from?
All FDA import refusal data for Flobeman 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.