GURUJI PRODUCTS PVT. LTD.
⚠️ High Risk
FEI: 2000030304 • Indore, Madhya Pradesh • INDIA
FEI Number
2000030304
Location
Indore, Madhya Pradesh
Country
INDIAAddress
285 Infront Of Bharat Petrol Pump, A B Road, Pigdambar, Indore, Madhya Pradesh, India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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.
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).
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.
COL ADDED
The article appears to bear or contain, for the purpose of coloring only, a color additive which is unsafe within the meaning of Section 721(a).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/1/2025 | 36BHT99SYRUPS AND MOLASSES, N.E.C. | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 5/4/2023 | 30YGT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | 274COLOR LBLG | Division of Northeast Imports (DNEI) |
| 8/13/2018 | 30BCT99FRUIT BEVERAGE BASES, LIQUID, N.E.C. | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 7/20/2018 | 36BCT99SYRUPS AND MOLASSES, N.E.C. | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 7/20/2018 | 36BCT99SYRUPS AND MOLASSES, N.E.C. | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 6/29/2015 | 36BHT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 6/29/2015 | 36BHT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 6/29/2015 | 36BHT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 6/29/2015 | 36BHT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 8/22/2013 | 36BHT99SYRUPS AND MOLASSES, N.E.C. | 11UNSAFE COL | New York District Office (NYK-DO) |
| 4/19/2011 | 36BCT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 4/19/2011 | 36BCT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 4/19/2011 | 36BCT99SYRUPS AND MOLASSES, N.E.C. | New York District Office (NYK-DO) | |
| 5/14/2009 | 30YGY99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 1/13/2009 | 30GCT99BEVERAGE BASE OF NON-FRUIT ORIGIN, LIQUID, N.E.C. | New York District Office (NYK-DO) | |
| 1/13/2009 | 30GCT99BEVERAGE BASE OF NON-FRUIT ORIGIN, LIQUID, N.E.C. | New York District Office (NYK-DO) | |
| 1/13/2009 | 30GCT99BEVERAGE BASE OF NON-FRUIT ORIGIN, LIQUID, N.E.C. | New York District Office (NYK-DO) | |
| 1/13/2009 | 30GCT99BEVERAGE BASE OF NON-FRUIT ORIGIN, LIQUID, N.E.C. | New York District Office (NYK-DO) | |
| 1/13/2009 | 30GCT99BEVERAGE BASE OF NON-FRUIT ORIGIN, LIQUID, N.E.C. | New York District Office (NYK-DO) | |
| 3/27/2007 | 66CAL99STOOL SOFTENER N.E.C. | San Francisco District Office (SAN-DO) | |
| 3/27/2007 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is GURUJI PRODUCTS PVT. LTD.'s FDA import refusal history?
GURUJI PRODUCTS PVT. LTD. (FEI: 2000030304) has 21 FDA import refusal record(s) in our database, spanning from 3/27/2007 to 10/1/2025.
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. GURUJI PRODUCTS PVT. LTD.'s FEI number is 2000030304.
What types of violations has GURUJI PRODUCTS PVT. LTD. received?
GURUJI PRODUCTS PVT. LTD. has been cited for 9 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 GURUJI PRODUCTS PVT. LTD. come from?
All FDA import refusal data for GURUJI PRODUCTS PVT. LTD. 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.