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Rabia & Company

⚠️ Moderate Risk

FEI: 3032903422 • Faridabad, Haryana • INDIA

FEI

FEI Number

3032903422

📍

Location

Faridabad, Haryana

🇮🇳

Country

INDIA
🏢

Address

house no 1079, main mathura road, Faridabad, Haryana, India

Moderate Risk

FDA Import Risk Assessment

46.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
1/30/2025
Latest Refusal
1/30/2025
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
11.2×30%
Recency
80.8×20%
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

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

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
1/30/2025
54JDY11BETEL NUT (HERBAL AND BOTANICAL TEAS II, CONTINUED)
238UNSAFE ADD
482NUTRIT LBL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Rabia & Company's FDA import refusal history?

Rabia & Company (FEI: 3032903422) has 1 FDA import refusal record(s) in our database, spanning from 1/30/2025 to 1/30/2025.

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. Rabia & Company's FEI number is 3032903422.

What types of violations has Rabia & Company received?

Rabia & Company 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 Rabia & Company come from?

All FDA import refusal data for Rabia & Company 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.