Dr.Anrian Ariawan
⚠️ Moderate Risk
FEI: 3005428319 • Jakartajakarta • INDONESIA
FEI Number
3005428319
Location
Jakartajakarta
Country
INDONESIAAddress
Kekapang Utara 1 No.1, , Jakartajakarta, , Indonesia
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
DRUG GMPS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/7/2005 | 54AFK13VITAMIN C (ASCORBIC ACID) | 27DRUG GMPS | Cincinnati District Office (CIN-DO) |
| 12/7/2005 | 60QDK67LIDOCAINE (ANESTHETIC) | 27DRUG GMPS | Cincinnati District Office (CIN-DO) |
| 12/7/2005 | 54AFK09COBALAMIN CONCENTRATE (VITAMIN) | 27DRUG GMPS | Cincinnati District Office (CIN-DO) |
| 12/7/2005 | 66VCA99MISCELLANEOUS PATENT MEDICINES, ETC. | 27DRUG GMPS | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Dr.Anrian Ariawan's FDA import refusal history?
Dr.Anrian Ariawan (FEI: 3005428319) has 4 FDA import refusal record(s) in our database, spanning from 12/7/2005 to 12/7/2005.
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. Dr.Anrian Ariawan's FEI number is 3005428319.
What types of violations has Dr.Anrian Ariawan received?
Dr.Anrian Ariawan 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 Dr.Anrian Ariawan come from?
All FDA import refusal data for Dr.Anrian Ariawan 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.