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Asoaroma

⚠️ Moderate Risk

FEI: 3007997339 • Rionegro, Antioquia • COLOMBIA

FEI

FEI Number

3007997339

📍

Location

Rionegro, Antioquia

🇨🇴

Country

COLOMBIA
🏢

Address

Barrio Porvenir, Carrera 65 No 45b-85, Rionegro, Antioquia, Colombia

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
1/9/2012
Latest Refusal
12/16/2011
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

2413×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
1/9/2012
28AGC04BASIL (SWEET BASIL), WHOLE (SPICE)
241PESTICIDE
Florida District Office (FLA-DO)
1/9/2012
28AGC04BASIL (SWEET BASIL), WHOLE (SPICE)
241PESTICIDE
Florida District Office (FLA-DO)
12/16/2011
28AGC04BASIL (SWEET BASIL), WHOLE (SPICE)
241PESTICIDE
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Asoaroma's FDA import refusal history?

Asoaroma (FEI: 3007997339) has 3 FDA import refusal record(s) in our database, spanning from 12/16/2011 to 1/9/2012.

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. Asoaroma's FEI number is 3007997339.

What types of violations has Asoaroma received?

Asoaroma 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 Asoaroma come from?

All FDA import refusal data for Asoaroma 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.