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Nortec Quimica SA

⚠️ Moderate Risk

FEI: 3007616930 • Duque De Caxias, Rio de Janeiro • BRAZIL

FEI

FEI Number

3007616930

📍

Location

Duque De Caxias, Rio de Janeiro

🇧🇷

Country

BRAZIL
🏢

Address

Rua Dezessete # 200, Dist. Ind. Duque De Caxias - Xerem, Duque De Caxias, Rio de Janeiro, Brazil

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/22/2011
Latest Refusal
5/17/2011
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

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).

Refusal History

DateProductViolationsDivision
6/22/2011
60WCS39THIABENDAZOLE (ANTHELMINTIC)
118NOT LISTED
Southwest Import District Office (SWI-DO)
5/17/2011
60WCS39THIABENDAZOLE (ANTHELMINTIC)
118NOT LISTED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Nortec Quimica SA's FDA import refusal history?

Nortec Quimica SA (FEI: 3007616930) has 2 FDA import refusal record(s) in our database, spanning from 5/17/2011 to 6/22/2011.

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. Nortec Quimica SA's FEI number is 3007616930.

What types of violations has Nortec Quimica SA received?

Nortec Quimica SA 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 Nortec Quimica SA come from?

All FDA import refusal data for Nortec Quimica SA 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.