PT GATRAKARSA ESTADAYA
⚠️ High Risk
FEI: 3007748639 • Jakarta, Jabotabek • INDONESIA
FEI Number
3007748639
Location
Jakarta, Jabotabek
Country
INDONESIAAddress
Jln. Kalibata Utara 12 B, , Jakarta, Jabotabek, 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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/23/2015 | 16AGD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 12/23/2015 | 16AGD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 12/23/2015 | 16AGD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 12/23/2015 | 16AGD45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is PT GATRAKARSA ESTADAYA's FDA import refusal history?
PT GATRAKARSA ESTADAYA (FEI: 3007748639) has 4 FDA import refusal record(s) in our database, spanning from 12/23/2015 to 12/23/2015.
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. PT GATRAKARSA ESTADAYA's FEI number is 3007748639.
What types of violations has PT GATRAKARSA ESTADAYA received?
PT GATRAKARSA ESTADAYA 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 PT GATRAKARSA ESTADAYA come from?
All FDA import refusal data for PT GATRAKARSA ESTADAYA 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.