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super exports

⚠️ Moderate Risk

FEI: 3014748523 • Via Anand, Gujarat • INDIA

FEI

FEI Number

3014748523

📍

Location

Via Anand, Gujarat

🇮🇳

Country

INDIA
🏢

Address

Shed C- 5/6, Gidc Estate, Vitthal Udyognagar, Via Anand, Gujarat, India

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

25
Total Refusals
20
Unique Violations
7/21/2010
Latest Refusal
1/7/2003
Earliest Refusal

Score Breakdown

Violation Severity
48.0×40%
Refusal Volume
52.4×30%
Recency
0.0×20%
Frequency
33.2×10%
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

4739×

LABELING

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

4826×

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.

2184×

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.

3284×

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.

753×

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).

4713×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

832×

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.

2492×

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.

2742×

COLOR LBLG

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

3202×

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.

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.

3242×

NO ENGLISH

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)).

4752×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

622×

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).

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.

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

4881×

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.

1181×

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).

4741×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

Refusal History

DateProductViolationsDivision
7/21/2010
21HAH05DATES, DRIED OR PASTE
249FILTHY
New York District Office (NYK-DO)
6/11/2008
03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C.
249FILTHY
New York District Office (NYK-DO)
9/14/2005
54FGT99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
482NUTRIT LBL
New York District Office (NYK-DO)
9/14/2005
53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New York District Office (NYK-DO)
9/14/2005
54EDY99HERBALS & BOTANICAL TEAS, N.E.C.
75UNAPPROVED
New York District Office (NYK-DO)
9/14/2005
66VBO99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)
6/20/2005
53FH02HAIR TINTS (HAIR COLORING PREPARATIONS)
471CSTIC LBLG
473LABELING
474COSMETLBLG
475COSMETLBLG
Division of Southeast Imports (DSEI)
6/20/2005
23KGT99EDIBLE SEEDS, N.E.C.
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
473LABELING
Division of Southeast Imports (DSEI)
6/20/2005
03YEY99OTHER BAKERY PRODUCTS, N.E.C.
218LIST INGRE
274COLOR LBLG
320LACKS FIRM
328USUAL NAME
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/20/2005
30YGT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
218LIST INGRE
258FLAVR LBLG
274COLOR LBLG
321LACKS N/C
324NO ENGLISH
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
5/27/2005
54EDT99HERBALS & BOTANICAL TEAS, N.E.C.
2300DIETARYLBL
Division of Southeast Imports (DSEI)
5/27/2005
54FER99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
488HEALTH C
Division of Southeast Imports (DSEI)
5/27/2005
60SAR03ALUMINA/MAGNESIA (ANTACID)
483DRUG NAME
Division of Southeast Imports (DSEI)
5/27/2005
53FD03HAIR RINSES (COLORING) (HAIR COLORING PREPARATIONS)
475COSMETLBLG
Division of Southeast Imports (DSEI)
5/27/2005
29CET04MIXED DRINKS (NONALCOHOLIC BEVERAGES)
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
5/27/2005
02EVY99WHEAT FLOUR, N.E.C.
473LABELING
Division of Southeast Imports (DSEI)
5/27/2005
34FFT03CHOCOLATE COVERED CANDY BAR, WITHOUT NUTS AND FRUIT
473LABELING
Division of Southeast Imports (DSEI)
5/27/2005
53LC01CLEANSING (COLD CREAMS, CLEANSING LOTIONS, LIQUIDS, PADS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
Division of Southeast Imports (DSEI)
5/27/2005
03YEY99OTHER BAKERY PRODUCTS, N.E.C.
328USUAL NAME
482NUTRIT LBL
Division of Southeast Imports (DSEI)
5/27/2005
07BGT99FRIED SNACK FOODS, N.E.C.
328USUAL NAME
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
5/27/2005
21TFT05MANGO, DRIED OR PASTE
324NO ENGLISH
473LABELING
Division of Southeast Imports (DSEI)
5/27/2005
27YCT06PEPPER SAUCE (HOT, MILD, ETC.)
218LIST INGRE
62NEEDS FCE
83NO PROCESS
Division of Southeast Imports (DSEI)
5/27/2005
66VCS99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/27/2005
27YCT06PEPPER SAUCE (HOT, MILD, ETC.)
62NEEDS FCE
83NO PROCESS
Division of Southeast Imports (DSEI)
1/7/2003
53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS)
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is super exports's FDA import refusal history?

super exports (FEI: 3014748523) has 25 FDA import refusal record(s) in our database, spanning from 1/7/2003 to 7/21/2010.

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. super exports's FEI number is 3014748523.

What types of violations has super exports received?

super exports has been cited for 20 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 super exports come from?

All FDA import refusal data for super exports 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.