Laboratorios Pharmagroup Sa De Cv
✅ Low Risk
FEI: 3007253176 • Tlajomulco de Zuniga, Jalisco • MEXICO
FEI Number
3007253176
Location
Tlajomulco de Zuniga, Jalisco
Country
MEXICOAddress
Carr. Guadalajara Chapala Km 24, , Tlajomulco de Zuniga, Jalisco, Mexico
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
Frequently Asked Questions
What is Laboratorios Pharmagroup Sa De Cv's FDA import refusal history?
Laboratorios Pharmagroup Sa De Cv (FEI: 3007253176) has 2 FDA import refusal record(s) in our database, spanning from 1/13/2009 to 1/13/2009.
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. Laboratorios Pharmagroup Sa De Cv's FEI number is 3007253176.
What types of violations has Laboratorios Pharmagroup Sa De Cv received?
Laboratorios Pharmagroup Sa De Cv 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 Laboratorios Pharmagroup Sa De Cv come from?
All FDA import refusal data for Laboratorios Pharmagroup Sa De Cv 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.