IMPORTADORA Y MANUFACTURER BRULUART
⚠️ High Risk
FEI: 3018998917 • San Francisco, COL • MEXICO
FEI Number
3018998917
Location
San Francisco, COL
Country
MEXICOAddress
Geranios No. 9, , San Francisco, COL, Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/16/2024 | 54AGK05VITAMIN B12 (CYANOCOBALAMIN) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 9/7/2023 | 62GDY90DICLOFENAC POTASSIUM (ANTI-INFLAMMATORY) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 10/5/2022 | 54YEY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 4/8/2022 | 54ADA05VITAMIN B12 (CYANOCOBALAMIN) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is IMPORTADORA Y MANUFACTURER BRULUART's FDA import refusal history?
IMPORTADORA Y MANUFACTURER BRULUART (FEI: 3018998917) has 4 FDA import refusal record(s) in our database, spanning from 4/8/2022 to 7/16/2024.
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. IMPORTADORA Y MANUFACTURER BRULUART's FEI number is 3018998917.
What types of violations has IMPORTADORA Y MANUFACTURER BRULUART received?
IMPORTADORA Y MANUFACTURER BRULUART 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 IMPORTADORA Y MANUFACTURER BRULUART come from?
All FDA import refusal data for IMPORTADORA Y MANUFACTURER BRULUART 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.