Edith Ramirez
⚠️ Moderate Risk
FEI: 3003622493 • Tonala • 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
DIETARY
The article purports to be or is represented for special dietary uses and its label does not appear to bear the nutritional information required by regulation.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/21/2002 | 54AYY99VITAMIN, N.E.C. | 262DIETARY | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Edith Ramirez's FDA import refusal history?
Edith Ramirez (FEI: 3003622493) has 1 FDA import refusal record(s) in our database, spanning from 6/21/2002 to 6/21/2002.
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. Edith Ramirez's FEI number is 3003622493.
What types of violations has Edith Ramirez received?
Edith Ramirez 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 Edith Ramirez come from?
All FDA import refusal data for Edith Ramirez 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.