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Meca, S.A.

⚠️ Moderate Risk

FEI: 1000650474 • Orotina • COSTA RICA

FEI

FEI Number

1000650474

📍

Location

Orotina

🇨🇷

Country

COSTA RICA
🏢

Address

Apartado 4021-108, , Orotina, , Costa Rica

Moderate Risk

FDA Import Risk Assessment

47.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/30/2013
Latest Refusal
4/6/2006
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
4.1×10%
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
7/30/2013
25JFC16CASSAVA (ROOT AND TUBER VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)
8/7/2006
25JFC06POTATO (ROOT & TUBER VEGETABLE)
241PESTICIDE
Florida District Office (FLA-DO)
4/6/2006
25JFC06POTATO (ROOT & TUBER VEGETABLE)
241PESTICIDE
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Meca, S.A.'s FDA import refusal history?

Meca, S.A. (FEI: 1000650474) has 3 FDA import refusal record(s) in our database, spanning from 4/6/2006 to 7/30/2013.

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. Meca, S.A.'s FEI number is 1000650474.

What types of violations has Meca, S.A. received?

Meca, S.A. 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 Meca, S.A. come from?

All FDA import refusal data for Meca, S.A. 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.