DIOSELINA MARTINEZ DE HINCAPIE
⚠️ Moderate Risk
FEI: 3014237859 • Medellin, Antioquia • COLOMBIA
FEI Number
3014237859
Location
Medellin, Antioquia
Country
COLOMBIAAddress
Cra 81 A 37 C - 32, , Medellin, Antioquia, Colombia
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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
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
Frequently Asked Questions
What is DIOSELINA MARTINEZ DE HINCAPIE's FDA import refusal history?
DIOSELINA MARTINEZ DE HINCAPIE (FEI: 3014237859) has 2 FDA import refusal record(s) in our database, spanning from 4/9/2018 to 4/9/2018.
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. DIOSELINA MARTINEZ DE HINCAPIE's FEI number is 3014237859.
What types of violations has DIOSELINA MARTINEZ DE HINCAPIE received?
DIOSELINA MARTINEZ DE HINCAPIE has been cited for 2 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 DIOSELINA MARTINEZ DE HINCAPIE come from?
All FDA import refusal data for DIOSELINA MARTINEZ DE HINCAPIE 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.