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UAB CANCHEMA

⚠️ Moderate Risk

FEI: 3040031932 • Vilnius, Vilnius County • LITHUANIA

FEI

FEI Number

3040031932

📍

Location

Vilnius, Vilnius County

🇱🇹

Country

LITHUANIA
🏢

Address

Piliakalnio G. 7, , Vilnius, Vilnius County, Lithuania

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
2
Unique Violations
11/6/2025
Latest Refusal
11/6/2025
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
11.2×30%
Recency
96.4×20%
Frequency
10.0×10%
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

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).

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

Refusal History

DateProductViolationsDivision
11/6/2025
60ZCY12FENBENDAZOLE (ANTIPARASITIC)
118NOT LISTED
2280DIRSEXMPT
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is UAB CANCHEMA's FDA import refusal history?

UAB CANCHEMA (FEI: 3040031932) has 1 FDA import refusal record(s) in our database, spanning from 11/6/2025 to 11/6/2025.

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. UAB CANCHEMA's FEI number is 3040031932.

What types of violations has UAB CANCHEMA received?

UAB CANCHEMA 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 UAB CANCHEMA come from?

All FDA import refusal data for UAB CANCHEMA 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.