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SGB & SONS

⚠️ High Risk

FEI: 3014782767 • Anand 38800 (Guji) • INDIA

FEI

FEI Number

3014782767

📍

Location

Anand 38800 (Guji)

🇮🇳

Country

INDIA
🏢

Address

Tarapurshottam Kutir, Tower Bazar, Anand 38800 (Guji), , India

High Risk

FDA Import Risk Assessment

58.4
LowModerateHighCritical

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

Statistics

9
Total Refusals
4
Unique Violations
9/5/2025
Latest Refusal
12/4/2018
Earliest Refusal

Score Breakdown

Violation Severity
75.4×40%
Refusal Volume
37.0×30%
Recency
78.8×20%
Frequency
13.3×10%
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

118×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2183×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2491×

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.

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

Refusal History

DateProductViolationsDivision
9/5/2025
03YGY13PAPAD
249FILTHY
Division of Northeast Imports (DNEI)
1/14/2019
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
274COLOR LBLG
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
218LIST INGRE
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
218LIST INGRE
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
218LIST INGRE
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
Division of West Coast Imports (DWCI)
12/4/2018
37BGN99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
11UNSAFE COL
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is SGB & SONS's FDA import refusal history?

SGB & SONS (FEI: 3014782767) has 9 FDA import refusal record(s) in our database, spanning from 12/4/2018 to 9/5/2025.

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. SGB & SONS's FEI number is 3014782767.

What types of violations has SGB & SONS received?

SGB & SONS has been cited for 4 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 SGB & SONS come from?

All FDA import refusal data for SGB & SONS 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.