Embotelladora De Monclova Sa
⚠️ Moderate Risk
FEI: 3003362008 • Monclova, Coahuila de Zaragoza • MEXICO
FEI Number
3003362008
Location
Monclova, Coahuila de Zaragoza
Country
MEXICOAddress
Avenida Venustiano Carranza 200, Col. Zona Centro, Monclova, Monclova, Coahuila de Zaragoza, Mexico
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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
Refusal History
Frequently Asked Questions
What is Embotelladora De Monclova Sa's FDA import refusal history?
Embotelladora De Monclova Sa (FEI: 3003362008) has 2 FDA import refusal record(s) in our database, spanning from 4/14/2003 to 4/27/2004.
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. Embotelladora De Monclova Sa's FEI number is 3003362008.
What types of violations has Embotelladora De Monclova Sa received?
Embotelladora De Monclova Sa 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 Embotelladora De Monclova Sa come from?
All FDA import refusal data for Embotelladora De Monclova Sa 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.