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S&R Exports

⚠️ Moderate Risk

FEI: 3001551123 • New Delhi, Delhi • INDIA

FEI

FEI Number

3001551123

📍

Location

New Delhi, Delhi

🇮🇳

Country

INDIA
🏢

Address

E4, , New Delhi, Delhi, India

Moderate Risk

FDA Import Risk Assessment

43.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
3/2/2007
Latest Refusal
5/14/2003
Earliest Refusal

Score Breakdown

Violation Severity
95.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
5.3×10%
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

1711×

CONTAINER

The container appears to be composed, in whole or in part, of a poisonous or deleterious substance which may render the contents injurious to health.

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.

Refusal History

DateProductViolationsDivision
3/2/2007
52AID53FRYING PAN, CAKE PAN, ETC., (SHALLOW ITEM CAPABLE OF HOLDING LIQUID, W/ OR W/O LID) (FOOD/COOK/TABLE
238UNSAFE ADD
New York District Office (NYK-DO)
5/14/2003
52AID34STORAGE CONTAINERS (W/ OR W/O LID), (FOODWARE, COOKWARE & TABLEWARE)
171CONTAINER
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is S&R Exports's FDA import refusal history?

S&R Exports (FEI: 3001551123) has 2 FDA import refusal record(s) in our database, spanning from 5/14/2003 to 3/2/2007.

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. S&R Exports's FEI number is 3001551123.

What types of violations has S&R Exports received?

S&R Exports 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 S&R Exports come from?

All FDA import refusal data for S&R Exports 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.