Fiavesa Imp Exp
⚠️ Moderate Risk
FEI: 3001397245 • Maracaibo • VENEZUELA
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
MFRHACCP
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).
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 |
|---|---|---|---|
| 5/9/2002 | 16JEO01CRAB | 249FILTHY | Florida District Office (FLA-DO) |
| 3/13/2002 | 16JEO01CRAB | 2580MFRHACCP | Florida District Office (FLA-DO) |
| 3/13/2002 | 16JEO01CRAB | 2580MFRHACCP | Florida District Office (FLA-DO) |
| 3/13/2002 | 16JEO01CRAB | 2580MFRHACCP | Florida District Office (FLA-DO) |
| 3/13/2002 | 16JEO01CRAB | 2580MFRHACCP | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Fiavesa Imp Exp's FDA import refusal history?
Fiavesa Imp Exp (FEI: 3001397245) has 5 FDA import refusal record(s) in our database, spanning from 3/13/2002 to 5/9/2002.
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. Fiavesa Imp Exp's FEI number is 3001397245.
What types of violations has Fiavesa Imp Exp received?
Fiavesa Imp Exp has been cited for 2 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 Fiavesa Imp Exp come from?
All FDA import refusal data for Fiavesa Imp Exp 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.