Abel Quintana H
⚠️ Moderate Risk
FEI: 3004950853 • Amanalco De Bec • MEXICO
FEI Number
3004950853
Location
Amanalco De Bec
Country
MEXICOAddress
Becerra No 512, , Amanalco De Bec, , 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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/4/2005 | 65VCA15DIAZEPAM (SEDATIVE) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 3/4/2005 | 66MCA03ALPRAZOLAM (TRANQUILIZER) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 3/4/2005 | 66MCA03ALPRAZOLAM (TRANQUILIZER) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 3/4/2005 | 61UCA05TAMOXIFEN CITRATE (ANTI-ESTROGEN) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 3/4/2005 | 64MCA01CLOMIPHENE CITRATE (GONAD-STIMULATING PRINCIPLE) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Abel Quintana H's FDA import refusal history?
Abel Quintana H (FEI: 3004950853) has 5 FDA import refusal record(s) in our database, spanning from 3/4/2005 to 3/4/2005.
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. Abel Quintana H's FEI number is 3004950853.
What types of violations has Abel Quintana H received?
Abel Quintana H 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 Abel Quintana H come from?
All FDA import refusal data for Abel Quintana H 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.