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ARPIT AGRO PRODUCTS

⚠️ High Risk

FEI: 3016919899 • Jalgaon • INDIA

FEI

FEI Number

3016919899

📍

Location

Jalgaon

🇮🇳

Country

INDIA
🏢

Address

F-69, Midc Area, , Jalgaon, , India

High Risk

FDA Import Risk Assessment

64.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
7/14/2025
Latest Refusal
6/5/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
75.3×20%
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
7/14/2025
24BGT09MUNG BEAN, DRIED OR PASTE
241PESTICIDE
Division of Northern Border Imports (DNBI)
6/5/2025
24BGT09MUNG BEAN, DRIED OR PASTE
241PESTICIDE
Division of Northern Border Imports (DNBI)
6/5/2025
24BGT09MUNG BEAN, DRIED OR PASTE
241PESTICIDE
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is ARPIT AGRO PRODUCTS's FDA import refusal history?

ARPIT AGRO PRODUCTS (FEI: 3016919899) has 3 FDA import refusal record(s) in our database, spanning from 6/5/2025 to 7/14/2025.

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. ARPIT AGRO PRODUCTS's FEI number is 3016919899.

What types of violations has ARPIT AGRO PRODUCTS received?

ARPIT AGRO PRODUCTS 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 ARPIT AGRO PRODUCTS come from?

All FDA import refusal data for ARPIT AGRO PRODUCTS 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.