M/s Dahyabhai Vithaldas
⚠️ Moderate Risk
FEI: 3004346132 • Ahmedabad, Gujarat • INDIA
FEI Number
3004346132
Location
Ahmedabad, Gujarat
Country
INDIAAddress
1450, New Madhavpura, O/S Delhi Gate, Ahmedabad, Gujarat, 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.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(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).
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.
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/15/2004 | 23KGT02SESAME SEED (EDIBLE SEED) | 249FILTHY | Atlanta District Office (ATL-DO) |
| 4/15/2004 | 21TGT14TAMARIND, DRIED OR PASTE | 249FILTHY | Atlanta District Office (ATL-DO) |
| 3/30/2004 | 62UBA99ANTI-TUSSIVE/COLD N.E.C. | 472NO ENGLISH | Atlanta District Office (ATL-DO) |
| 3/8/2004 | 60SBL99ANTACID, N.E.C. | 472NO ENGLISH | Atlanta District Office (ATL-DO) |
| 3/8/2004 | 60SBL99ANTACID, N.E.C. | 75UNAPPROVED | Atlanta District Office (ATL-DO) |
| 3/8/2004 | 64ABL99DISINFECTANT N.E.C. | 75UNAPPROVED | Atlanta District Office (ATL-DO) |
| 10/10/2003 | 28BGT08CAPSICUMS (CAYENNE CHILI, HOT PEPPERS), GROUND, CRACKED (SPICE) | 9SALMONELLA | Atlanta District Office (ATL-DO) |
| 6/24/2003 | 33YGT99CANDY WITHOUT CHOCOLATE N.E.C. | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is M/s Dahyabhai Vithaldas's FDA import refusal history?
M/s Dahyabhai Vithaldas (FEI: 3004346132) has 8 FDA import refusal record(s) in our database, spanning from 6/24/2003 to 6/15/2004.
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. M/s Dahyabhai Vithaldas's FEI number is 3004346132.
What types of violations has M/s Dahyabhai Vithaldas received?
M/s Dahyabhai Vithaldas has been cited for 6 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 M/s Dahyabhai Vithaldas come from?
All FDA import refusal data for M/s Dahyabhai Vithaldas 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.