AKSHAR IMPEX
⚠️ High Risk
FEI: 3013248129 • Mumbai, Maharashtra • INDIA
FEI Number
3013248129
Location
Mumbai, Maharashtra
Country
INDIAAddress
B-106, CHITRA APT., S.N. ROAD,, TAMBE NAGAR, MULUND (W), Mumbai, Maharashtra, 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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it 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.
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.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
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:
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.
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.
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.
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/18/2024 | 28BGT16CUMIN, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 10/26/2023 | 23BGT14BETEL NUT, SHELLED | 3878POISONORD | Division of Northeast Imports (DNEI) |
| 10/26/2023 | 23BGT14BETEL NUT, SHELLED | 3878POISONORD | Division of Northeast Imports (DNEI) |
| 10/26/2023 | 23BGT14BETEL NUT, SHELLED | 3878POISONORD | Division of Northeast Imports (DNEI) |
| 10/26/2023 | 23BGT14BETEL NUT, SHELLED | 3878POISONORD | Division of Northeast Imports (DNEI) |
| 7/27/2022 | 21TCT14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 6/29/2022 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) | |
| 6/29/2022 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Division of Northeast Imports (DNEI) | |
| 6/29/2022 | 23KGT02SESAME SEED (EDIBLE SEED) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 6/29/2022 | 23KGT02SESAME SEED (EDIBLE SEED) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 12/21/2020 | 23KGT02SESAME SEED (EDIBLE SEED) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 8/14/2017 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 8/14/2017 | 28AGT54PEPPER,BLACK, WHOLE (SPICE) | 9SALMONELLA | Division of Northeast Imports (DNEI) |
| 7/24/2017 | 30YGT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 7/24/2017 | 65RAY18SODIUM BICARBONATE (REPLENISHER) | Division of Northeast Imports (DNEI) | |
| 4/20/2017 | 26CGT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 309FORBIDDEN | Division of Northeast Imports (DNEI) |
| 6/6/2016 | 28OCT99ESSENTIAL OILS FOR FLAVORING, N.E.C. | 218LIST INGRE | Division of Northeast Imports (DNEI) |
| 6/6/2016 | 28OCT99ESSENTIAL OILS FOR FLAVORING, N.E.C. | 218LIST INGRE | Division of Northeast Imports (DNEI) |
| 6/6/2016 | 28OCT99ESSENTIAL OILS FOR FLAVORING, N.E.C. | 218LIST INGRE | Division of Northeast Imports (DNEI) |
| 2/3/2016 | 21UCP14TAMARIND, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 249FILTHY | New York District Office (NYK-DO) |
| 2/23/2015 | 21UCP14TAMARIND, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED | 249FILTHY | Division of Northeast Imports (DNEI) |
| 5/18/2012 | 21TGH14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 5/18/2012 | 21TGH14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Northeast Imports (DNEI) |
| 5/18/2012 | 26ACT12MUSTARD OIL, CRUDE, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 5/18/2012 | 26ACT12MUSTARD OIL, CRUDE, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 5/18/2012 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 5/18/2012 | 66VCS99MISCELLANEOUS PATENT MEDICINES, ETC. | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 2/16/2012 | 54IBR02PSYLLIUM (FIBER) | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/16/2012 | 54IBR02PSYLLIUM (FIBER) | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 2/16/2012 | 26CGT12RAPESEED/CANOLA OIL, REFINED, SINGLE INGREDIENT | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 2/16/2012 | 09AET02BUTTER OIL | New York District Office (NYK-DO) | |
| 2/16/2012 | 09AET02BUTTER OIL | New York District Office (NYK-DO) | |
| 2/16/2012 | 60SKL99ANTACID, N.E.C. | 118NOT LISTED | New York District Office (NYK-DO) |
| 8/16/2011 | 53LD01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS) | 75UNAPPROVED | New York District Office (NYK-DO) |
| 7/1/2008 | 28BGT08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE) | 249FILTHY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is AKSHAR IMPEX's FDA import refusal history?
AKSHAR IMPEX (FEI: 3013248129) has 35 FDA import refusal record(s) in our database, spanning from 7/1/2008 to 6/18/2024.
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. AKSHAR IMPEX's FEI number is 3013248129.
What types of violations has AKSHAR IMPEX received?
AKSHAR IMPEX has been cited for 15 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 AKSHAR IMPEX come from?
All FDA import refusal data for AKSHAR IMPEX 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.