MARIA DEL CARMEN OBANDO LAZARO
⚠️ Moderate Risk
FEI: 3016985633 • Palmira, Valle Del Cauca • COLOMBIA
FEI Number
3016985633
Location
Palmira, Valle Del Cauca
Country
COLOMBIAAddress
Carrera 12 38 17, , Palmira, Valle Del Cauca, 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
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 |
|---|---|---|---|
| 7/17/2020 | 62ODA41LOSARTAN POTASSIUM (ANTI-HYPERTENSIVE - PART II) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is MARIA DEL CARMEN OBANDO LAZARO's FDA import refusal history?
MARIA DEL CARMEN OBANDO LAZARO (FEI: 3016985633) has 1 FDA import refusal record(s) in our database, spanning from 7/17/2020 to 7/17/2020.
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. MARIA DEL CARMEN OBANDO LAZARO's FEI number is 3016985633.
What types of violations has MARIA DEL CARMEN OBANDO LAZARO received?
MARIA DEL CARMEN OBANDO LAZARO 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 MARIA DEL CARMEN OBANDO LAZARO come from?
All FDA import refusal data for MARIA DEL CARMEN OBANDO LAZARO 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.