ImportRefusal LogoImportRefusal

Sunstar Broadline Distribution

⚠️ High Risk

FEI: 3010269709 • New Delhi, Delhi • INDIA

FEI

FEI Number

3010269709

📍

Location

New Delhi, Delhi

🇮🇳

Country

INDIA
🏢

Address

1st Floor, 4119/7, New Delhi, Delhi, India

High Risk

FDA Import Risk Assessment

61.7
LowModerateHighCritical

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

Statistics

14
Total Refusals
2
Unique Violations
3/20/2014
Latest Refusal
7/18/2013
Earliest Refusal

Score Breakdown

Violation Severity
96.5×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

24911×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

37216×

PESTICIDE2

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

Refusal History

DateProductViolationsDivision
3/20/2014
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
3721PESTICIDE2
Los Angeles District Office (LOS-DO)
2/21/2014
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Atlanta District Office (ATL-DO)
2/21/2014
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Atlanta District Office (ATL-DO)
2/21/2014
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Atlanta District Office (ATL-DO)
1/7/2014
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Division of Northeast Imports (DNEI)
12/11/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Division of West Coast Imports (DWCI)
11/1/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
3721PESTICIDE2
San Francisco District Office (SAN-DO)
9/5/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
3721PESTICIDE2
Southwest Import District Office (SWI-DO)
9/5/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
3721PESTICIDE2
Southwest Import District Office (SWI-DO)
9/5/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Southwest Import District Office (SWI-DO)
9/5/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
3721PESTICIDE2
Southwest Import District Office (SWI-DO)
8/30/2013
02DGT07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
3721PESTICIDE2
Seattle District Office (SEA-DO)
7/18/2013
02DAB07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Los Angeles District Office (LOS-DO)
7/18/2013
02DAB07RICE, BASMATI, PROCESSED (PACKAGED)
249FILTHY
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Sunstar Broadline Distribution's FDA import refusal history?

Sunstar Broadline Distribution (FEI: 3010269709) has 14 FDA import refusal record(s) in our database, spanning from 7/18/2013 to 3/20/2014.

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. Sunstar Broadline Distribution's FEI number is 3010269709.

What types of violations has Sunstar Broadline Distribution received?

Sunstar Broadline Distribution 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 Sunstar Broadline Distribution come from?

All FDA import refusal data for Sunstar Broadline Distribution 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.