Gaivotaprateada Lda.
⚠️ High Risk
FEI: 3012136889 • Condeixa A Nova, Coimbra • PORTUGAL
FEI Number
3012136889
Location
Condeixa A Nova, Coimbra
Country
PORTUGALAddress
Sao Fipo, Ega, Rua Principal No. 49 51, Condeixa A Nova, Coimbra, Portugal
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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 |
|---|---|---|---|
| 4/26/2022 | 16MGD09OCTOPUS, OTHER AQUATIC SPECIES | 249FILTHY | Division of Southeast Imports (DSEI) |
| 4/26/2022 | 16MGD09OCTOPUS, OTHER AQUATIC SPECIES | 249FILTHY | Division of Southeast Imports (DSEI) |
| 4/26/2022 | 16MGD09OCTOPUS, OTHER AQUATIC SPECIES | 249FILTHY | Division of Southeast Imports (DSEI) |
| 4/26/2022 | 16MGD09OCTOPUS, OTHER AQUATIC SPECIES | 249FILTHY | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Gaivotaprateada Lda.'s FDA import refusal history?
Gaivotaprateada Lda. (FEI: 3012136889) has 4 FDA import refusal record(s) in our database, spanning from 4/26/2022 to 4/26/2022.
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. Gaivotaprateada Lda.'s FEI number is 3012136889.
What types of violations has Gaivotaprateada Lda. received?
Gaivotaprateada Lda. 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 Gaivotaprateada Lda. come from?
All FDA import refusal data for Gaivotaprateada Lda. 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.