Antillana S.A.
⚠️ Moderate Risk
FEI: 1000304091 • Cartagena • COLOMBIA
FEI Number
1000304091
Location
Cartagena
Country
COLOMBIAAddress
1923 Manga, , Cartagena, , Colombia
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/5/2010 | 16JGD06SPINY LOBSTER, ROCK LOBSTER | 249FILTHY | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Antillana S.A.'s FDA import refusal history?
Antillana S.A. (FEI: 1000304091) has 1 FDA import refusal record(s) in our database, spanning from 2/5/2010 to 2/5/2010.
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. Antillana S.A.'s FEI number is 1000304091.
What types of violations has Antillana S.A. received?
Antillana S.A. 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 Antillana S.A. come from?
All FDA import refusal data for Antillana S.A. 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.