RUTH STELLA GARCIA CLEVES
⚠️ Moderate Risk
FEI: 3017359899 • Cali, Valle Del Cauca • COLOMBIA
FEI Number
3017359899
Location
Cali, Valle Del Cauca
Country
COLOMBIAAddress
Carrera 19 33f 44, , Cali, 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
Frequently Asked Questions
What is RUTH STELLA GARCIA CLEVES's FDA import refusal history?
RUTH STELLA GARCIA CLEVES (FEI: 3017359899) has 2 FDA import refusal record(s) in our database, spanning from 10/28/2020 to 10/28/2020.
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. RUTH STELLA GARCIA CLEVES's FEI number is 3017359899.
What types of violations has RUTH STELLA GARCIA CLEVES received?
RUTH STELLA GARCIA CLEVES 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 RUTH STELLA GARCIA CLEVES come from?
All FDA import refusal data for RUTH STELLA GARCIA CLEVES 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.