Taio Marine Services Limited
⚠️ Moderate Risk
FEI: 3003820305 • Rarotonga • COOK ISLANDS
FEI Number
3003820305
Location
Rarotonga
Country
COOK ISLANDSAddress
P.O. Box 2001, , Rarotonga, , Cook Islands
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
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
Frequently Asked Questions
What is Taio Marine Services Limited's FDA import refusal history?
Taio Marine Services Limited (FEI: 3003820305) has 2 FDA import refusal record(s) in our database, spanning from 2/7/2005 to 2/14/2005.
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. Taio Marine Services Limited's FEI number is 3003820305.
What types of violations has Taio Marine Services Limited received?
Taio Marine Services Limited 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 Taio Marine Services Limited come from?
All FDA import refusal data for Taio Marine Services Limited 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.