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ASOFARMA DE MEXICO S A DE CV

⚠️ High Risk

FEI: 3016889706 • San Lorenzo Hup • MEXICO

FEI

FEI Number

3016889706

📍

Location

San Lorenzo Hup

🇲🇽

Country

MEXICO
🏢

Address

Calz Mexicoxochimilco N, , San Lorenzo Hup, , Mexico

High Risk

FDA Import Risk Assessment

51.4
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
3/22/2023
Latest Refusal
11/10/2022
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
28.8×20%
Frequency
30.0×10%
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

753×

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

DateProductViolationsDivision
3/22/2023
66VDR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/1/2023
65PDA03TAMSULOSIN HCL (REGULATOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/10/2022
54YDF99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ASOFARMA DE MEXICO S A DE CV's FDA import refusal history?

ASOFARMA DE MEXICO S A DE CV (FEI: 3016889706) has 3 FDA import refusal record(s) in our database, spanning from 11/10/2022 to 3/22/2023.

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. ASOFARMA DE MEXICO S A DE CV's FEI number is 3016889706.

What types of violations has ASOFARMA DE MEXICO S A DE CV received?

ASOFARMA DE MEXICO S A 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 ASOFARMA DE MEXICO S A DE CV come from?

All FDA import refusal data for ASOFARMA DE MEXICO S A 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.