Cv. Ratu Aroma
⚠️ High Risk
FEI: 3010710236 • Banten • INDONESIA
FEI Number
3010710236
Location
Banten
Country
INDONESIAAddress
Block A2, No 13, C, , Banten, , Indonesia
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
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 |
|---|---|---|---|
| 1/9/2026 | 28OEY99ESSENTIAL OILS FOR FLAVORING, N.E.C. | 308MFR INSAN | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Cv. Ratu Aroma's FDA import refusal history?
Cv. Ratu Aroma (FEI: 3010710236) has 1 FDA import refusal record(s) in our database, spanning from 1/9/2026 to 1/9/2026.
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. Cv. Ratu Aroma's FEI number is 3010710236.
What types of violations has Cv. Ratu Aroma received?
Cv. Ratu Aroma 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 Cv. Ratu Aroma come from?
All FDA import refusal data for Cv. Ratu Aroma 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.