super exports
⚠️ Moderate Risk
FEI: 3014748523 • Via Anand, Gujarat • INDIA
FEI Number
3014748523
Location
Via Anand, Gujarat
Country
INDIAAddress
Shed C- 5/6, Gidc Estate, Vitthal Udyognagar, Via Anand, Gujarat, India
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
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.
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).
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.
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.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
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.
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)).
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.
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).
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.
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.
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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) | Division of Southeast Imports (DSEI) | |
| 6/20/2005 | 23KGT99EDIBLE SEEDS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/20/2005 | 03YEY99OTHER BAKERY PRODUCTS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 6/20/2005 | 30YGT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | 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) | 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. | Division of Southeast Imports (DSEI) | |
| 5/27/2005 | 07BGT99FRIED SNACK FOODS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 5/27/2005 | 21TFT05MANGO, DRIED OR PASTE | Division of Southeast Imports (DSEI) | |
| 5/27/2005 | 27YCT06PEPPER SAUCE (HOT, MILD, ETC.) | 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.) | 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.