Dabur India Limited
⚠️ Moderate Risk
FEI: 3008450520 • Tonk, Rajasthan • INDIA
FEI Number
3008450520
Location
Tonk, Rajasthan
Country
INDIAAddress
Plot No. G-50-59, IID Center, Road No. 1, NH-12, Newai, Tonk, Rajasthan, 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
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).
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.
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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/16/2019 | 22KGT01POMEGRANATE, JUICE, OTHER FRUIT JUICES OR CONCENTRATES | 11UNSAFE COL | Division of Northern Border Imports (DNBI) |
| 1/9/2017 | 36CHT04HONEY | 320LACKS FIRM | Division of Northeast Imports (DNEI) |
| 8/30/2011 | 21VDT99SUTROPICAL AND TROPICAL FRUIT, JUICE, MILK, CREME, DRINK OR NECTAR, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT04GUAVA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT99SUTROPICAL AND TROPICAL FRUIT, JUICE, MILK, CREME, DRINK OR NECTAR, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) | |
| 8/30/2011 | 21VDT04GUAVA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Dabur India Limited's FDA import refusal history?
Dabur India Limited (FEI: 3008450520) has 10 FDA import refusal record(s) in our database, spanning from 8/30/2011 to 9/16/2019.
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. Dabur India Limited's FEI number is 3008450520.
What types of violations has Dabur India Limited received?
Dabur India Limited has been cited for 4 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 Dabur India Limited come from?
All FDA import refusal data for Dabur India Limited 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.