ImportRefusal LogoImportRefusal

PSICOFARMA

⚠️ High Risk

FEI: 3004086663 • C.P. • MEXICO

FEI

FEI Number

3004086663

📍

Location

C.P.

🇲🇽

Country

MEXICO
🏢

Address

S.A. DE C.V. Calz. de Tialpan No. 4369, Col. Toliello Guerra, Deleg. Tialpan,C.P., , Mexico

High Risk

FDA Import Risk Assessment

56.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
1/21/2026
Latest Refusal
7/20/2022
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
17.7×30%
Recency
98.0×20%
Frequency
5.7×10%
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

752×

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).

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
1/21/2026
61KDA10BIPERIDEN (ANTI-CHOLINERGIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/20/2022
61NCY29FLUOXETINE (ANTI-DEPRESSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PSICOFARMA's FDA import refusal history?

PSICOFARMA (FEI: 3004086663) has 2 FDA import refusal record(s) in our database, spanning from 7/20/2022 to 1/21/2026.

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. PSICOFARMA's FEI number is 3004086663.

What types of violations has PSICOFARMA received?

PSICOFARMA has been cited for 2 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 PSICOFARMA come from?

All FDA import refusal data for PSICOFARMA 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.