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COLLINS S.A.

⚠️ High Risk

FEI: 3005575198 • GUADALAJARA • MEXICO

FEI

FEI Number

3005575198

📍

Location

GUADALAJARA

🇲🇽

Country

MEXICO
🏢

Address

CIPRES NO. 1677, , GUADALAJARA, , Mexico

High Risk

FDA Import Risk Assessment

63.9
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
1/2/2026
Latest Refusal
12/17/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
90.7×20%
Frequency
19.5×10%
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

754×

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
1/2/2026
56CDY70CEFTRIAXONE SODIUM (CEPHALOSPORINS)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/2/2026
64LDL19DEXAMETHASONE (GLUCOCORTICOID)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/17/2023
61WCY46ITRACONAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/17/2023
61FCY30DICLOXACILLIN (ANTI-BACTERIAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is COLLINS S.A.'s FDA import refusal history?

COLLINS S.A. (FEI: 3005575198) has 4 FDA import refusal record(s) in our database, spanning from 12/17/2023 to 1/2/2026.

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. COLLINS S.A.'s FEI number is 3005575198.

What types of violations has COLLINS S.A. received?

COLLINS S.A. 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 COLLINS S.A. come from?

All FDA import refusal data for COLLINS S.A. 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.