Bansal Export Inc.
⚠️ Moderate Risk
FEI: 3002727439 • New Delhi, Delhi • INDIA
FEI Number
3002727439
Location
New Delhi, Delhi
Country
INDIAAddress
6048/3, , New Delhi, Delhi, 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
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.
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.
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.
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.
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.
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).
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).
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.
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.
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).
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/22/2005 | 07BGT99FRIED SNACK FOODS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 8/22/2005 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | San Francisco District Office (SAN-DO) | |
| 8/10/2004 | 60FBR03TALC (ADSORBANT) | 118NOT LISTED | Baltimore District Office (BLT-DO) |
| 8/10/2004 | 60FBR03TALC (ADSORBANT) | 118NOT LISTED | Baltimore District Office (BLT-DO) |
| 2/27/2004 | 03CET99BREADS, ROLLS, BUNS, ETC N.E.C. PREPARED DRY MIX WITHOUT MILK OR EGG | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 2/27/2004 | 03CET99BREADS, ROLLS, BUNS, ETC N.E.C. PREPARED DRY MIX WITHOUT MILK OR EGG | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 2/27/2004 | 03CET99BREADS, ROLLS, BUNS, ETC N.E.C. PREPARED DRY MIX WITHOUT MILK OR EGG | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 2/27/2004 | 03CET99BREADS, ROLLS, BUNS, ETC N.E.C. PREPARED DRY MIX WITHOUT MILK OR EGG | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 3/19/2003 | 28SFT99SALT (TABLE SALT) N.E.C. | 75UNAPPROVED | San Francisco District Office (SAN-DO) |
| 3/7/2003 | 07AGT99BAKED SNACK FOOD, N.E.C. | San Francisco District Office (SAN-DO) | |
| 3/7/2003 | 03CET99BREADS, ROLLS, BUNS, ETC N.E.C. PREPARED DRY MIX WITHOUT MILK OR EGG | 83NO PROCESS | San Francisco District Office (SAN-DO) |
| 2/13/2002 | 21TGT02BANANA, DRIED OR PASTE | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Bansal Export Inc.'s FDA import refusal history?
Bansal Export Inc. (FEI: 3002727439) has 12 FDA import refusal record(s) in our database, spanning from 2/13/2002 to 8/22/2005.
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. Bansal Export Inc.'s FEI number is 3002727439.
What types of violations has Bansal Export Inc. received?
Bansal Export Inc. has been cited for 13 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 Bansal Export Inc. come from?
All FDA import refusal data for Bansal Export Inc. 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.