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IMRG GLOBAL

⚠️ Moderate Risk

FEI: 3012576454 • New Delhi, Delhi • INDIA

FEI

FEI Number

3012576454

📍

Location

New Delhi, Delhi

🇮🇳

Country

INDIA
🏢

Address

N9 Golden Leaf House, , New Delhi, Delhi, India

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
7/13/2017
Latest Refusal
7/13/2017
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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:

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
7/13/2017
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
241PESTICIDE
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is IMRG GLOBAL's FDA import refusal history?

IMRG GLOBAL (FEI: 3012576454) has 1 FDA import refusal record(s) in our database, spanning from 7/13/2017 to 7/13/2017.

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. IMRG GLOBAL's FEI number is 3012576454.

What types of violations has IMRG GLOBAL received?

IMRG GLOBAL 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 IMRG GLOBAL come from?

All FDA import refusal data for IMRG GLOBAL 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.