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unknown

⚠️ High Risk

FEI: 3001056209 • unknown • INDIA

FEI

FEI Number

3001056209

📍

Location

unknown

🇮🇳

Country

INDIA
🏢

Address

unknown, , unknown, , India

High Risk

FDA Import Risk Assessment

62.3
LowModerateHighCritical

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

Statistics

34
Total Refusals
17
Unique Violations
9/30/2025
Latest Refusal
2/14/2002
Earliest Refusal

Score Breakdown

Violation Severity
62.2×40%
Refusal Volume
57.2×30%
Recency
94.1×20%
Frequency
14.4×10%
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

758×

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).

3218×

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.

2387×

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.

4825×

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.

32805×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

114×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2494×

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.

2744×

COLOR LBLG

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

94×

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.

3203×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

4733×

LABELING

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

2183×

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.

1183×

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).

2602×

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.

3282×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

22802×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

33001×

ALLERGEN

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

Refusal History

DateProductViolationsDivision
9/30/2025
23BGY14BETEL NUT, SHELLED
238UNSAFE ADD
320LACKS FIRM
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/30/2025
23BGY14BETEL NUT, SHELLED
238UNSAFE ADD
Division of Northeast Imports (DNEI)
9/30/2025
23BGY14BETEL NUT, SHELLED
218LIST INGRE
238UNSAFE ADD
320LACKS FIRM
321LACKS N/C
3300ALLERGEN
Division of Northeast Imports (DNEI)
9/24/2025
26CHT09SESAME OIL, REFINED, SINGLE INGREDIENT
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
7/31/2025
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/31/2025
53ED07TONICS, DRESSINGS, AND OTHER HAIR GROOMING AIDS (HAIR PREPARATIONS, NON-COLORING)
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
7/16/2025
60CDA09PHENYLEPHRINE HCL (ADRENERGIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/20/2024
23BGY14BETEL NUT, SHELLED
238UNSAFE ADD
Division of Northeast Imports (DNEI)
9/11/2024
26CCT01COCONUT OIL, REFINED, SINGLE INGREDIENT
473LABELING
Division of Northeast Imports (DNEI)
9/3/2024
33EYT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/3/2024
33EYT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/3/2024
34YGY99CHOCOLATE AND COCOA PRODUCTS, N.E.C.
321LACKS N/C
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/3/2024
23BGY14BETEL NUT, SHELLED
238UNSAFE ADD
Division of Northeast Imports (DNEI)
9/3/2024
33EYT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
218LIST INGRE
321LACKS N/C
Division of Northeast Imports (DNEI)
9/3/2024
33EYT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
218LIST INGRE
321LACKS N/C
Division of Northeast Imports (DNEI)
9/3/2024
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
9/3/2024
33EYT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)
9/3/2024
33EGY99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)
9/3/2024
28AGY18FENNEL, WHOLE (SPICE)
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)
9/3/2024
33EYT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)
6/6/2024
28CHT99NATURAL EXTRACT OR FLAVOR, N.E.C.
238UNSAFE ADD
75UNAPPROVED
Division of Northeast Imports (DNEI)
6/4/2024
28CGT99NATURAL EXTRACT OR FLAVOR, N.E.C.
238UNSAFE ADD
Division of Northeast Imports (DNEI)
12/16/2020
54YEY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
12/16/2020
62LCA23AMODIAQUINE HCL (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
118NOT LISTED
2280DIRSEXMPT
3280FRNMFGREG
75UNAPPROVED
Division of Northeast Imports (DNEI)
10/4/2019
03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
473LABELING
Division of Southeast Imports (DSEI)
10/4/2019
03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
473LABELING
Division of Southeast Imports (DSEI)
8/17/2018
63VBJ02HYDROQUINONE (DEPIGMENTOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/28/2018
62GBJ99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
Division of Northeast Imports (DNEI)
3/19/2007
07AGT99BAKED SNACK FOOD, N.E.C.
260FALSE
328USUAL NAME
Los Angeles District Office (LOS-DO)
3/19/2007
07AGT99BAKED SNACK FOOD, N.E.C.
260FALSE
328USUAL NAME
Los Angeles District Office (LOS-DO)
3/17/2006
28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
249FILTHY
9SALMONELLA
Detroit District Office (DET-DO)
6/26/2002
28BFT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
249FILTHY
9SALMONELLA
Detroit District Office (DET-DO)
4/17/2002
28AGT54PEPPER,BLACK, WHOLE (SPICE)
249FILTHY
320LACKS FIRM
9SALMONELLA
Detroit District Office (DET-DO)
2/14/2002
28AHT54PEPPER,BLACK, WHOLE (SPICE)
249FILTHY
9SALMONELLA
Detroit District Office (DET-DO)

Frequently Asked Questions

What is unknown's FDA import refusal history?

unknown (FEI: 3001056209) has 34 FDA import refusal record(s) in our database, spanning from 2/14/2002 to 9/30/2025.

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. unknown's FEI number is 3001056209.

What types of violations has unknown received?

unknown has been cited for 17 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 unknown come from?

All FDA import refusal data for unknown 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.