GOLDEN INDIA EXPOTRADE PVT. LTD
⚠️ Moderate Risk
FEI: 3009165976 • 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.
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.
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.
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.
ALLERGEN
the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).
PRESRV LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a chemical preservative and it fails to bear labeling stating that fact including its function.
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/12/2015 | 29BET02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED | Los Angeles District Office (LOS-DO) | |
| 11/12/2015 | 04CGT99NOODLES AND NOODLE PRODUCTS, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03HGT07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03HGT07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03AGT03BISCUITS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03AGT03BISCUITS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03AGT03BISCUITS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03HGT07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03HGT07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03HGT07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) | |
| 11/6/2015 | 03HGT07MIXED PLAIN COOKIES,BISCUITS AND WAFERS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is GOLDEN INDIA EXPOTRADE PVT. LTD's FDA import refusal history?
GOLDEN INDIA EXPOTRADE PVT. LTD (FEI: 3009165976) has 11 FDA import refusal record(s) in our database, spanning from 11/6/2015 to 11/12/2015.
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. GOLDEN INDIA EXPOTRADE PVT. LTD's FEI number is 3009165976.
What types of violations has GOLDEN INDIA EXPOTRADE PVT. LTD received?
GOLDEN INDIA EXPOTRADE PVT. LTD has been cited for 7 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 GOLDEN INDIA EXPOTRADE PVT. LTD come from?
All FDA import refusal data for GOLDEN INDIA EXPOTRADE 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.