ImportRefusal LogoImportRefusal

Peter Peters Guenter

⚠️ Moderate Risk

FEI: 3010494475 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3010494475

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Domicilio Conocido Campo, Barrio Barrio Oxtopulco Universidad, Coyoacan, Ciudad De Mexico, Ciudad de Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/25/2013
Latest Refusal
11/25/2013
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2411×

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
11/25/2013
24FJB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Peter Peters Guenter's FDA import refusal history?

Peter Peters Guenter (FEI: 3010494475) has 1 FDA import refusal record(s) in our database, spanning from 11/25/2013 to 11/25/2013.

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. Peter Peters Guenter's FEI number is 3010494475.

What types of violations has Peter Peters Guenter received?

Peter Peters Guenter 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 Peter Peters Guenter come from?

All FDA import refusal data for Peter Peters Guenter 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.