R.S.LAL INTERNATIONAL
⚠️ Moderate Risk
FEI: 3004292378 • New Delhi, Delhi • INDIA
FEI Number
3004292378
Location
New Delhi, Delhi
Country
INDIAAddress
285 Swarn Park Udyog Nagar, , 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
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.
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.
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.
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.
JUICE %
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 the food purports to be a beverage containing vegetable or fruit juice and does not bear a statement on the label in appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained therein.
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.
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.
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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).
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).
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/6/2011 | 28AGT54PEPPER,BLACK, WHOLE (SPICE) | Chicago District Office (CHI-DO) | |
| 6/6/2011 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 9SALMONELLA | Chicago District Office (CHI-DO) |
| 6/2/2011 | 33EGY99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | San Francisco District Office (SAN-DO) | |
| 4/12/2010 | 28BGH08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE) | San Francisco District Office (SAN-DO) | |
| 1/26/2010 | 22DCT07WINTER MELON, JUICE, VINE FRUIT JUICES OR CONCENTRATES | San Francisco District Office (SAN-DO) | |
| 1/26/2010 | 22DCT05BITTER MELON, JUICE, VINE FRUIT JUICES OR CONCENTRATES | San Francisco District Office (SAN-DO) | |
| 1/26/2010 | 29ACT99NONCARBONATED SOFT DRINK, N.E.C. | San Francisco District Office (SAN-DO) | |
| 9/11/2009 | 28BGY54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Chicago District Office (CHI-DO) | |
| 12/1/2008 | 33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 482NUTRIT LBL | San Francisco District Office (SAN-DO) |
| 12/1/2008 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 12/1/2008 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 12/1/2008 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 12/1/2008 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 12/1/2008 | 03HGT99PLAIN COOKIES,BISCUITS AND WAFERS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 12/14/2007 | 18CGT99COMBINATION MEAT-LIKE VEGETABLE PROTEIN PRODUCTS, N.E.C. | San Francisco District Office (SAN-DO) | |
| 8/7/2007 | 60LAR99ANALGESIC, N.E.C. | San Francisco District Office (SAN-DO) | |
| 7/9/2007 | 28BGH19GINGER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 1/24/2005 | 28BGT30NUTMEG, GROUND, CRACKED (SPICE) | San Francisco District Office (SAN-DO) | |
| 1/24/2005 | 28AGT15CORIANDER, WHOLE (SPICE) | San Francisco District Office (SAN-DO) | |
| 10/27/2004 | 33GGT12MIXED/ASSORTED SOFT CANDY WITH NUTS, NUT PRODUCTS, OR SEEDS W/O COCONUT OR CHOCOLATE | Los Angeles District Office (LOS-DO) | |
| 5/19/2004 | 28BFT49TURMERIC, GROUND, CRACKED (SPICE) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is R.S.LAL INTERNATIONAL's FDA import refusal history?
R.S.LAL INTERNATIONAL (FEI: 3004292378) has 21 FDA import refusal record(s) in our database, spanning from 5/19/2004 to 6/6/2011.
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. R.S.LAL INTERNATIONAL's FEI number is 3004292378.
What types of violations has R.S.LAL INTERNATIONAL received?
R.S.LAL INTERNATIONAL has been cited for 16 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 R.S.LAL INTERNATIONAL come from?
All FDA import refusal data for R.S.LAL INTERNATIONAL 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.