Xiamen C And D Inc.
⚠️ Moderate Risk
FEI: 3004079512 • Xiamen • CHINA
FEI Number
3004079512
Location
Xiamen
Country
CHINAAddress
22th Flr., Seaside Bldg, , Xiamen, , China
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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/22/2007 | 16AFN15EEL | 2920PESTICIDES | Los Angeles District Office (LOS-DO) |
| 5/22/2007 | 16AFN15EEL | 238UNSAFE ADD | Los Angeles District Office (LOS-DO) |
| 5/22/2007 | 16AFN15EEL | 238UNSAFE ADD | Los Angeles District Office (LOS-DO) |
| 5/22/2007 | 16AFN15EEL | 238UNSAFE ADD | Los Angeles District Office (LOS-DO) |
| 5/22/2007 | 16AFN15EEL | 238UNSAFE ADD | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Xiamen C And D Inc.'s FDA import refusal history?
Xiamen C And D Inc. (FEI: 3004079512) has 5 FDA import refusal record(s) in our database, spanning from 5/22/2007 to 5/22/2007.
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. Xiamen C And D Inc.'s FEI number is 3004079512.
What types of violations has Xiamen C And D Inc. received?
Xiamen C And D Inc. 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 Xiamen C And D Inc. come from?
All FDA import refusal data for Xiamen C And D Inc. 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.