F.Loendersloot Internationale expeditie
⚠️ Moderate Risk
FEI: 3010787256 • Roosendaal, Noord-Brabant • NETHERLANDS
FEI Number
3010787256
Location
Roosendaal, Noord-Brabant
Country
NETHERLANDSAddress
Kooldreef 7, , Roosendaal, Noord-Brabant, Netherlands
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
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 |
|---|---|---|---|
| 7/29/2005 | 79FRODRESSING, WOUND, DRUG | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
| 7/29/2005 | 80KGXTAPE AND BANDAGE, ADHESIVE | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
| 7/29/2005 | 79FRODRESSING, WOUND, DRUG | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
| 7/29/2005 | 79FPXSTRIP, ADHESIVE, CLOSURE, SKIN | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is F.Loendersloot Internationale expeditie's FDA import refusal history?
F.Loendersloot Internationale expeditie (FEI: 3010787256) has 4 FDA import refusal record(s) in our database, spanning from 7/29/2005 to 7/29/2005.
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. F.Loendersloot Internationale expeditie's FEI number is 3010787256.
What types of violations has F.Loendersloot Internationale expeditie received?
F.Loendersloot Internationale expeditie 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 F.Loendersloot Internationale expeditie come from?
All FDA import refusal data for F.Loendersloot Internationale expeditie 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.