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Produlab Pharma

⚠️ High Risk

FEI: 3008224438 • Raamsdonksveer, Noord-Brabant • NETHERLANDS

FEI

FEI Number

3008224438

📍

Location

Raamsdonksveer, Noord-Brabant

🇳🇱
🏢

Address

Forellenweg 16, , Raamsdonksveer, Noord-Brabant, Netherlands

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
11/10/2025
Latest Refusal
6/8/2011
Earliest Refusal

Score Breakdown

Violation Severity
61.1×40%
Refusal Volume
25.9×30%
Recency
96.7×20%
Frequency
2.8×10%
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

724×

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.

1182×

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).

32802×

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.

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

Refusal History

DateProductViolationsDivision
11/10/2025
60ZPL15IVERMECTIN AND COMBINATIONS (ANTIPARASITIC)
118NOT LISTED
3280FRNMFGREG
72NEW VET DR
Division of West Coast Imports (DWCI)
11/10/2025
60ZPL15IVERMECTIN AND COMBINATIONS (ANTIPARASITIC)
118NOT LISTED
3280FRNMFGREG
72NEW VET DR
Division of West Coast Imports (DWCI)
11/16/2016
68YAK99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
3260NO ENGLISH
72NEW VET DR
Division of Southeast Imports (DSEI)
6/8/2011
66MQO99TRANQUILIZER N.E.C.
72NEW VET DR
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Produlab Pharma's FDA import refusal history?

Produlab Pharma (FEI: 3008224438) has 4 FDA import refusal record(s) in our database, spanning from 6/8/2011 to 11/10/2025.

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. Produlab Pharma's FEI number is 3008224438.

What types of violations has Produlab Pharma received?

Produlab Pharma has been cited for 4 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 Produlab Pharma come from?

All FDA import refusal data for Produlab Pharma 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.