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AFRIMA DE MICHOACAN

✅ Low Risk

FEI: 3009196902 • Morelia, Michoacan de Ocampo • MEXICO

FEI

FEI Number

3009196902

📍

Location

Morelia, Michoacan de Ocampo

🇲🇽

Country

MEXICO
🏢

Address

Calle Benito Juarez 1205, Col. Granjas Del Maestro, Morelia, Morelia, Michoacan de Ocampo, Mexico

Low Risk

FDA Import Risk Assessment

22.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
6/29/2010
Latest Refusal
6/29/2010
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
6/29/2010
07BGT02CORN CHIPS, FRIED
260FALSE
482NUTRIT LBL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is AFRIMA DE MICHOACAN's FDA import refusal history?

AFRIMA DE MICHOACAN (FEI: 3009196902) has 1 FDA import refusal record(s) in our database, spanning from 6/29/2010 to 6/29/2010.

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. AFRIMA DE MICHOACAN's FEI number is 3009196902.

What types of violations has AFRIMA DE MICHOACAN received?

AFRIMA DE MICHOACAN has been cited for 2 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 AFRIMA DE MICHOACAN come from?

All FDA import refusal data for AFRIMA DE MICHOACAN 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.