Jocafe S.A. De C.V
⚠️ Moderate Risk
FEI: 3003914460 • N.L. • MEXICO
FEI Number
3003914460
Location
N.L.
Country
MEXICOAddress
Romulo Diaz De La Vega No. #, , Monterrey, N.L., , 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
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/3/2004 | 29WCY02BOTTLED SPRING OR MINERAL WATER | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Jocafe S.A. De C.V's FDA import refusal history?
Jocafe S.A. De C.V (FEI: 3003914460) has 1 FDA import refusal record(s) in our database, spanning from 9/3/2004 to 9/3/2004.
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. Jocafe S.A. De C.V's FEI number is 3003914460.
What types of violations has Jocafe S.A. De C.V received?
Jocafe S.A. De C.V 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 Jocafe S.A. De C.V come from?
All FDA import refusal data for Jocafe S.A. De C.V 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.