ImportRefusal LogoImportRefusal

CANCHEMA UAB

⚠️ High Risk

FEI: 3022109408 • Vilnius • LITHUANIA

FEI

FEI Number

3022109408

📍

Location

Vilnius

🇱🇹

Country

LITHUANIA
🏢

Address

V Maciuleviciaus 51, , Vilnius, , Lithuania

High Risk

FDA Import Risk Assessment

65.6
LowModerateHighCritical

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

Statistics

20
Total Refusals
5
Unique Violations
6/28/2023
Latest Refusal
11/23/2022
Earliest Refusal

Score Breakdown

Violation Severity
77.6×40%
Refusal Volume
49.0×30%
Recency
49.2×20%
Frequency
100.0×10%
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

7519×

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).

1184×

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).

32804×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

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.

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
6/28/2023
60ZOH12FENBENDAZOLE (ANTIPARASITIC)
118NOT LISTED
3280FRNMFGREG
72NEW VET DR
Division of Southeast Imports (DSEI)
2/3/2023
41YYY99DIETARY CONVENTIONAL FOODS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/31/2023
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/3/2023
65CIR09SODIUM PHENYLBUTYRATE (NUTRIENT/TONIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/3/2023
65CAR09SODIUM PHENYLBUTYRATE (NUTRIENT/TONIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/23/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/21/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
60ZOY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/13/2022
65COY09SODIUM PHENYLBUTYRATE (NUTRIENT/TONIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/23/2022
60ZPY12FENBENDAZOLE (ANTIPARASITIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is CANCHEMA UAB's FDA import refusal history?

CANCHEMA UAB (FEI: 3022109408) has 20 FDA import refusal record(s) in our database, spanning from 11/23/2022 to 6/28/2023.

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. CANCHEMA UAB's FEI number is 3022109408.

What types of violations has CANCHEMA UAB received?

CANCHEMA UAB has been cited for 5 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 CANCHEMA UAB come from?

All FDA import refusal data for CANCHEMA UAB 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.