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NOBLE DEHYDRATES

⚠️ High Risk

FEI: 3012892172 • Distt. Jhalawar, Rajasthan • INDIA

FEI

FEI Number

3012892172

📍

Location

Distt. Jhalawar, Rajasthan

🇮🇳

Country

INDIA
🏢

Address

6th KM Stone, Aklera-Kota, NH 52, Maithoon, , Distt. Jhalawar, Rajasthan, India

High Risk

FDA Import Risk Assessment

66.6
LowModerateHighCritical

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

Statistics

10
Total Refusals
3
Unique Violations
8/11/2025
Latest Refusal
4/26/2016
Earliest Refusal

Score Breakdown

Violation Severity
89.1×40%
Refusal Volume
38.6×30%
Recency
91.7×20%
Frequency
10.8×10%
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

2497×

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.

3153×

ADDED BULK

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the food appears to have a substance added to, mixed or packed with it so as to increase its bulk or weight, or reduce its quality or strength, or make it appear better or of greater value than it is.

2181×

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.

Refusal History

DateProductViolationsDivision
8/11/2025
20KCT04LEMON, CITRUS FRUIT JUICES OR CONCENTRATES
315ADDED BULK
Division of Southwest Imports (DSWI)
8/11/2025
20KCT04LEMON, CITRUS FRUIT JUICES OR CONCENTRATES
315ADDED BULK
Division of Southwest Imports (DSWI)
1/2/2025
20KCT04LEMON, CITRUS FRUIT JUICES OR CONCENTRATES
218LIST INGRE
315ADDED BULK
Division of West Coast Imports (DWCI)
3/23/2022
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
3/23/2022
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
3/23/2022
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
3/23/2022
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
3/23/2022
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)
6/30/2020
21THN14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northern Border Imports (DNBI)
4/26/2016
21TCT14TAMARIND, DRIED OR PASTE
249FILTHY
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is NOBLE DEHYDRATES's FDA import refusal history?

NOBLE DEHYDRATES (FEI: 3012892172) has 10 FDA import refusal record(s) in our database, spanning from 4/26/2016 to 8/11/2025.

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. NOBLE DEHYDRATES's FEI number is 3012892172.

What types of violations has NOBLE DEHYDRATES received?

NOBLE DEHYDRATES has been cited for 3 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 NOBLE DEHYDRATES come from?

All FDA import refusal data for NOBLE DEHYDRATES 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.