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NESTLE INDIA LIMITED

⚠️ Moderate Risk

FEI: 3013477077 • Mysore, Kartanaka • INDIA

FEI

FEI Number

3013477077

📍

Location

Mysore, Kartanaka

🇮🇳

Country

INDIA
🏢

Address

Kiadb Industrial Area, Nanjangud, , Mysore, Kartanaka, India

Moderate Risk

FDA Import Risk Assessment

40.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
7
Unique Violations
11/8/2024
Latest Refusal
11/28/2016
Earliest Refusal

Score Breakdown

Violation Severity
53.8×40%
Refusal Volume
22.3×30%
Recency
61.5×20%
Frequency
3.8×10%
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

33002×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

2581×

FLAVR LBLG

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an artificial flavoring and it fails to bear labeling stating that fact.

2741×

COLOR LBLG

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

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.

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

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
11/8/2024
04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C.
3300ALLERGEN
Division of West Coast Imports (DWCI)
11/8/2024
04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C.
3300ALLERGEN
Division of West Coast Imports (DWCI)
11/28/2016
04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C.
218LIST INGRE
258FLAVR LBLG
274COLOR LBLG
3320TRANSFAT
473LABELING
482NUTRIT LBL
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is NESTLE INDIA LIMITED's FDA import refusal history?

NESTLE INDIA LIMITED (FEI: 3013477077) has 3 FDA import refusal record(s) in our database, spanning from 11/28/2016 to 11/8/2024.

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. NESTLE INDIA LIMITED's FEI number is 3013477077.

What types of violations has NESTLE INDIA LIMITED received?

NESTLE INDIA LIMITED has been cited for 7 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 NESTLE INDIA LIMITED come from?

All FDA import refusal data for NESTLE INDIA LIMITED 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.