TECNOFARMA SA DE CV
⚠️ Moderate Risk
FEI: 3013338414 • Granjas • 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 |
|---|---|---|---|
| 11/22/2019 | 60ZCA15IVERMECTIN AND COMBINATIONS (ANTIPARASITIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 9/23/2019 | 61ADH07CLAMOXYQUIN HCL (ANTI-AMEBIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 4/5/2019 | 66KCA01METHIMAZOLE (THYROID INHIBITOR) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 5/8/2018 | 60ZCA15IVERMECTIN AND COMBINATIONS (ANTIPARASITIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is TECNOFARMA SA DE CV's FDA import refusal history?
TECNOFARMA SA DE CV (FEI: 3013338414) has 4 FDA import refusal record(s) in our database, spanning from 5/8/2018 to 11/22/2019.
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. TECNOFARMA SA DE CV's FEI number is 3013338414.
What types of violations has TECNOFARMA SA DE CV received?
TECNOFARMA 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 TECNOFARMA SA DE CV come from?
All FDA import refusal data for TECNOFARMA 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.