Tastel
⚠️ Moderate Risk
FEI: 3003978644 • Mumbai, Maharashtra • INDIA
FEI Number
3003978644
Location
Mumbai, Maharashtra
Country
INDIAAddress
220/E Sher Epunjab, Namlesh Apts 368/4, Mumbai, Maharashtra, 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
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/4/2005 | 03JGT99FILLED/ICED COOKIES,BISCUITS AND WAFERS, N.E.C. | 238UNSAFE ADD | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Tastel's FDA import refusal history?
Tastel (FEI: 3003978644) has 1 FDA import refusal record(s) in our database, spanning from 2/4/2005 to 2/4/2005.
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. Tastel's FEI number is 3003978644.
What types of violations has Tastel received?
Tastel has been cited for 1 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 Tastel come from?
All FDA import refusal data for Tastel 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.