Pd Setia Mandiri
⚠️ Moderate Risk
FEI: 3004972705 • Jakarta • INDONESIA
FEI Number
3004972705
Location
Jakarta
Country
INDONESIAAddress
Ji Asem No 9, , Jakarta, , 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/11/2006 | 37JGT03CHILI SAUCE | 482NUTRIT LBL | Los Angeles District Office (LOS-DO) |
| 7/27/2005 | 28JGE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 7/27/2005 | 28JGE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 7/27/2005 | 28JGE99MIXED SPICES AND SEASONING WITH SALT, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Pd Setia Mandiri's FDA import refusal history?
Pd Setia Mandiri (FEI: 3004972705) has 4 FDA import refusal record(s) in our database, spanning from 7/27/2005 to 5/11/2006.
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. Pd Setia Mandiri's FEI number is 3004972705.
What types of violations has Pd Setia Mandiri received?
Pd Setia Mandiri 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 Pd Setia Mandiri come from?
All FDA import refusal data for Pd Setia Mandiri 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.