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AKSHAR IMPEX

⚠️ High Risk

FEI: 3013248129 • Mumbai, Maharashtra • INDIA

FEI

FEI Number

3013248129

📍

Location

Mumbai, Maharashtra

🇮🇳

Country

INDIA
🏢

Address

B-106, CHITRA APT., S.N. ROAD,, TAMBE NAGAR, MULUND (W), Mumbai, Maharashtra, India

High Risk

FDA Import Risk Assessment

62.7
LowModerateHighCritical

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

Statistics

35
Total Refusals
15
Unique Violations
6/18/2024
Latest Refusal
7/1/2008
Earliest Refusal

Score Breakdown

Violation Severity
73.8×40%
Refusal Volume
57.6×30%
Recency
68.4×20%
Frequency
21.9×10%
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

98×

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.

2498×

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.

2186×

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.

1184×

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).

38784×

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:

4824×

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.

2383×

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.

3212×

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.

1572×

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.

752×

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).

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.

161×

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.

2741×

COLOR LBLG

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

3091×

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.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
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)
157FOREIGN OB
249FILTHY
9SALMONELLA
Division of Northeast Imports (DNEI)
6/29/2022
28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
157FOREIGN OB
249FILTHY
9SALMONELLA
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.
218LIST INGRE
258FLAVR LBLG
274COLOR LBLG
473LABELING
Division of Northeast Imports (DNEI)
7/24/2017
65RAY18SODIUM BICARBONATE (REPLENISHER)
118NOT LISTED
16DIRECTIONS
75UNAPPROVED
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
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
2/16/2012
09AET02BUTTER OIL
218LIST INGRE
321LACKS N/C
482NUTRIT LBL
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.