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GANESHA WORLDWIDE LLP

⚠️ High Risk

FEI: 3013884328 • Vadodara, Gujarat • INDIA

FEI

FEI Number

3013884328

📍

Location

Vadodara, Gujarat

🇮🇳

Country

INDIA
🏢

Address

C - 410 Sunrise Heights, Near South West Mall Atladara, Vadodara, Gujarat, India

High Risk

FDA Import Risk Assessment

53.4
LowModerateHighCritical

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

Statistics

6
Total Refusals
6
Unique Violations
3/20/2025
Latest Refusal
12/1/2017
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
31.3×30%
Recency
69.3×20%
Frequency
8.2×10%
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

114×

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).

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.

2741×

COLOR LBLG

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

3211×

LACKS N/C

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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

38781×

POISONORD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. 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
3/20/2025
23YGY99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
274COLOR LBLG
321LACKS N/C
482NUTRIT LBL
Division of West Coast Imports (DWCI)
11/3/2023
23OGT14BETEL NUT, NUT FLOUR/MEAL
238UNSAFE ADD
3878POISONORD
Division of West Coast Imports (DWCI)
5/24/2019
28BET10CARDAMON, GROUND, CRACKED (SPICE)
11UNSAFE COL
Division of Northeast Imports (DNEI)
5/24/2019
28BET10CARDAMON, GROUND, CRACKED (SPICE)
11UNSAFE COL
Division of Northeast Imports (DNEI)
5/24/2019
28BET10CARDAMON, GROUND, CRACKED (SPICE)
11UNSAFE COL
Division of Northeast Imports (DNEI)
12/1/2017
28BET10CARDAMON, GROUND, CRACKED (SPICE)
11UNSAFE COL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is GANESHA WORLDWIDE LLP's FDA import refusal history?

GANESHA WORLDWIDE LLP (FEI: 3013884328) has 6 FDA import refusal record(s) in our database, spanning from 12/1/2017 to 3/20/2025.

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. GANESHA WORLDWIDE LLP's FEI number is 3013884328.

What types of violations has GANESHA WORLDWIDE LLP received?

GANESHA WORLDWIDE LLP has been cited for 6 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 GANESHA WORLDWIDE LLP come from?

All FDA import refusal data for GANESHA WORLDWIDE LLP 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.