Grandways
⚠️ Moderate Risk
FEI: 3004843500 • New Delhi, Delhi • INDIA
FEI Number
3004843500
Location
New Delhi, Delhi
Country
INDIAAddress
C 85 Road No 40, , 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
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.
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.
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.
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.
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.
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/12/2009 | 20BGI08GOOSEBERRIES, DRIED OR PASTE | 238UNSAFE ADD | Seattle District Office (SEA-DO) |
| 4/22/2008 | 53FD01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI | Seattle District Office (SEA-DO) | |
| 4/22/2008 | 21SCT05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Seattle District Office (SEA-DO) | |
| 4/22/2008 | 21SCT05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Seattle District Office (SEA-DO) | |
| 4/22/2008 | 21SCT05MANGO (SUBTROPICAL AND TROPICAL FRUIT) | Seattle District Office (SEA-DO) | |
| 8/2/2005 | 02DGT07RICE, BASMATI, PROCESSED (PACKAGED) | 249FILTHY | Seattle District Office (SEA-DO) |
| 4/25/2005 | 28BGH54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Seattle District Office (SEA-DO) | |
| 4/25/2005 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Seattle District Office (SEA-DO) | |
| 4/25/2005 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Grandways's FDA import refusal history?
Grandways (FEI: 3004843500) has 9 FDA import refusal record(s) in our database, spanning from 4/25/2005 to 3/12/2009.
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. Grandways's FEI number is 3004843500.
What types of violations has Grandways received?
Grandways 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 Grandways come from?
All FDA import refusal data for Grandways 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.