Wahya Jatmiko
⚠️ Moderate Risk
FEI: 3003911330 • Medan • INDONESIA
FEI Number
3003911330
Location
Medan
Country
INDONESIAAddress
J1 D.I. Panjaitan 18, , Medan, , 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
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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/5/2003 | 79FSMTRAY, SURGICAL, INSTRUMENT | San Francisco District Office (SAN-DO) | |
| 3/5/2003 | 86HNRFORCEPS, OPHTHALMIC | San Francisco District Office (SAN-DO) | |
| 3/5/2003 | 86KYBLENS, GUIDE, INTRAOCULAR | San Francisco District Office (SAN-DO) | |
| 3/5/2003 | 86HMXCANNULA, OPHTHALMIC | San Francisco District Office (SAN-DO) | |
| 3/5/2003 | 86KYBLENS, GUIDE, INTRAOCULAR | San Francisco District Office (SAN-DO) | |
| 3/5/2003 | 86HNRFORCEPS, OPHTHALMIC | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Wahya Jatmiko's FDA import refusal history?
Wahya Jatmiko (FEI: 3003911330) has 6 FDA import refusal record(s) in our database, spanning from 3/5/2003 to 3/5/2003.
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. Wahya Jatmiko's FEI number is 3003911330.
What types of violations has Wahya Jatmiko received?
Wahya Jatmiko has been cited for 2 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 Wahya Jatmiko come from?
All FDA import refusal data for Wahya Jatmiko 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.