Agni Exim Private Limited
⚠️ High Risk
FEI: 3013836457 • Nayabasti, Kathmandu • NEPAL
FEI Number
3013836457
Location
Nayabasti, Kathmandu
Country
NEPALAddress
Gokarneshwor-5, , Nayabasti, Kathmandu, Nepal
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
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.
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.
STD IDENT
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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.
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.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/11/2025 | 28CET99NATURAL EXTRACT OR FLAVOR, N.E.C. | 83NO PROCESS | Division of Northeast Imports (DNEI) |
| 6/11/2025 | 37KCP99PASTES, N.E.C. | 83NO PROCESS | Division of Northeast Imports (DNEI) |
| 6/11/2025 | 28CET99NATURAL EXTRACT OR FLAVOR, N.E.C. | 83NO PROCESS | Division of Northeast Imports (DNEI) |
| 10/8/2021 | 21SCT14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT) | Division of Northeast Imports (DNEI) | |
| 10/8/2021 | 21SGY14TAMARIND (SUBTROPICAL AND TROPICAL FRUIT) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Agni Exim Private Limited's FDA import refusal history?
Agni Exim Private Limited (FEI: 3013836457) has 5 FDA import refusal record(s) in our database, spanning from 10/8/2021 to 6/11/2025.
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. Agni Exim Private Limited's FEI number is 3013836457.
What types of violations has Agni Exim Private Limited received?
Agni Exim Private Limited 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 Agni Exim Private Limited come from?
All FDA import refusal data for Agni Exim Private 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.