Atlantic Corporation
⚠️ Moderate Risk
FEI: 3003273269 • Mumbai • INDIA
FEI Number
3003273269
Location
Mumbai
Country
INDIAAddress
Unit No 111,1st Fl, A-2 Shah &Naher, , Mumbai, , 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.
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/30/2004 | 21TCT14TAMARIND, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
| 1/30/2004 | 21TCT14TAMARIND, DRIED OR PASTE | 249FILTHY | New York District Office (NYK-DO) |
| 1/30/2004 | 26CCT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 1/30/2004 | 26CCT11MUSTARD OIL, REFINED, SINGLE INGREDIENT, SEE 28O FOR MUSTARD OIL AS A FLAVORING | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 12/19/2002 | 65RBZ18SODIUM BICARBONATE (REPLENISHER) | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Atlantic Corporation's FDA import refusal history?
Atlantic Corporation (FEI: 3003273269) has 5 FDA import refusal record(s) in our database, spanning from 12/19/2002 to 1/30/2004.
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. Atlantic Corporation's FEI number is 3003273269.
What types of violations has Atlantic Corporation received?
Atlantic Corporation has been cited for 3 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 Atlantic Corporation come from?
All FDA import refusal data for Atlantic Corporation 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.