pt central pertiwi bahari plant I
⚠️ Moderate Risk
FEI: 3009208583 • Tanjung Bintang (sub district), Lampung • INDONESIA
FEI Number
3009208583
Location
Tanjung Bintang (sub district), Lampung
Country
INDONESIAAddress
Kawasan Industri, Jl. IR. Sutami KM.16, Tanjung Bintang (sub district), Lampung, 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
VETDRUGRES
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/21/2011 | 16XGD21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | 2860VETDRUGRES | Division of Southeast Imports (DSEI) |
| 3/21/2011 | 16XGD21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | 2860VETDRUGRES | Division of Southeast Imports (DSEI) |
| 3/21/2011 | 16XGT21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | 2860VETDRUGRES | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is pt central pertiwi bahari plant I's FDA import refusal history?
pt central pertiwi bahari plant I (FEI: 3009208583) has 3 FDA import refusal record(s) in our database, spanning from 3/21/2011 to 3/21/2011.
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 central pertiwi bahari plant I's FEI number is 3009208583.
What types of violations has pt central pertiwi bahari plant I received?
pt central pertiwi bahari plant I 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 central pertiwi bahari plant I come from?
All FDA import refusal data for pt central pertiwi bahari plant I 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.