Thai Nippon Rubber Industry Co., Ltd.
⚠️ High Risk
FEI: 3008808138 • Si Racha • THAILAND
FEI Number
3008808138
Location
Si Racha
Country
THAILANDAddress
789/139 Moo 1 Pinthong Industrial Estate, Nongkham, Si Racha, , Thailand
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
HOLES
The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.
Refusal History
Frequently Asked Questions
What is Thai Nippon Rubber Industry Co., Ltd.'s FDA import refusal history?
Thai Nippon Rubber Industry Co., Ltd. (FEI: 3008808138) has 4 FDA import refusal record(s) in our database, spanning from 7/2/2024 to 12/30/2024.
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. Thai Nippon Rubber Industry Co., Ltd.'s FEI number is 3008808138.
What types of violations has Thai Nippon Rubber Industry Co., Ltd. received?
Thai Nippon Rubber Industry Co., Ltd. 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 Thai Nippon Rubber Industry Co., Ltd. come from?
All FDA import refusal data for Thai Nippon Rubber Industry Co., Ltd. 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.