Jonathan Atiapa
⚠️ Moderate Risk
FEI: 3007844856 • Accra • GHANA
FEI Number
3007844856
Location
Accra
Country
GHANAAddress
3 South Liberia Roadadabraka, , Accra, , Ghana
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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/6/2009 | 16AFH99FISH, N.E.C. | 308MFR INSAN | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Jonathan Atiapa's FDA import refusal history?
Jonathan Atiapa (FEI: 3007844856) has 1 FDA import refusal record(s) in our database, spanning from 11/6/2009 to 11/6/2009.
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. Jonathan Atiapa's FEI number is 3007844856.
What types of violations has Jonathan Atiapa received?
Jonathan Atiapa 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 Jonathan Atiapa come from?
All FDA import refusal data for Jonathan Atiapa 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.