C&A Product Co., Ltd.
⚠️ Moderate Risk
FEI: 3003117742 • Mueang Nonthaburi, Nonthaburi • THAILAND
FEI Number
3003117742
Location
Mueang Nonthaburi, Nonthaburi
Country
THAILANDAddress
Ngamwongwarn 9 Alley 36/4/1 Ngam Wong Wan Soi, , Mueang Nonthaburi, Nonthaburi, Thailand
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.
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
Frequently Asked Questions
What is C&A Product Co., Ltd.'s FDA import refusal history?
C&A Product Co., Ltd. (FEI: 3003117742) has 2 FDA import refusal record(s) in our database, spanning from 7/24/2003 to 10/21/2004.
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. C&A Product Co., Ltd.'s FEI number is 3003117742.
What types of violations has C&A Product Co., Ltd. received?
C&A Product Co., Ltd. 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 C&A Product Co., Ltd. come from?
All FDA import refusal data for C&A Product 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.