Nestle India
⚠️ High Risk
FEI: 3014205794 • New Delhi • INDIA
FEI Number
3014205794
Location
New Delhi
Country
INDIAAddress
100/101, World Trade Centre, Barakhamba Lane, , New Delhi, , India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
INCONSPICU
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
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.
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.
FORBIDDEN
The article is subject to refusal of admission pursuant to Section 801(a)(2) in that it appears to be forbidden or restricted in sale in the country in which it was produced or from which it was exported.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
COLORLABEL
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use.
HEALTH C
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 bears an unauthorized nutrient content/health claim.
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/8/2025 | 21SYH14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT) | 249FILTHY | Division of Southeast Imports (DSEI) |
| 4/21/2025 | 04CGT07NOODLES, INSTANT | 238UNSAFE ADD | Division of West Coast Imports (DWCI) |
| 4/21/2025 | 04CGT07NOODLES, INSTANT | 238UNSAFE ADD | Division of West Coast Imports (DWCI) |
| 4/21/2025 | 04CGT07NOODLES, INSTANT | 238UNSAFE ADD | Division of West Coast Imports (DWCI) |
| 4/3/2025 | 04CGT07NOODLES, INSTANT | Division of Northeast Imports (DNEI) | |
| 4/2/2025 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 4/2/2025 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 2/20/2025 | 04CGT07NOODLES, INSTANT | 260FALSE | Division of Northeast Imports (DNEI) |
| 2/20/2025 | 04CGT07NOODLES, INSTANT | 260FALSE | Division of Northeast Imports (DNEI) |
| 12/23/2024 | 04CGT07NOODLES, INSTANT | Division of Southwest Imports (DSWI) | |
| 10/29/2024 | 04CGT07NOODLES, INSTANT | Division of Northeast Imports (DNEI) | |
| 4/1/2024 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 260FALSE | Division of Northern Border Imports (DNBI) |
| 12/6/2023 | 40BGH20MIXED CEREAL, WITH FRUIT (BABY) | 482NUTRIT LBL | Division of Northeast Imports (DNEI) |
| 3/17/2023 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 3/17/2023 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 3/17/2023 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 3/17/2023 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Division of Northern Border Imports (DNBI) | |
| 3/17/2023 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 256INCONSPICU | Division of Northern Border Imports (DNBI) |
| 2/9/2022 | 02YGT99MILLED GRAIN PRODUCTS, N.E.C. | Division of West Coast Imports (DWCI) | |
| 12/13/2021 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 249FILTHY | Division of West Coast Imports (DWCI) |
| 12/6/2021 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 249FILTHY | Division of West Coast Imports (DWCI) |
| 10/21/2021 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 249FILTHY | Division of West Coast Imports (DWCI) |
| 10/1/2021 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
| 10/1/2021 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | 249FILTHY | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Nestle India's FDA import refusal history?
Nestle India (FEI: 3014205794) has 24 FDA import refusal record(s) in our database, spanning from 10/1/2021 to 10/8/2025.
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. Nestle India's FEI number is 3014205794.
What types of violations has Nestle India received?
Nestle India has been cited for 13 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 come from?
All FDA import refusal data for Nestle India 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.