Faience Dap
⚠️ Moderate Risk
FEI: 3003461234 • Apt • FRANCE
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/20/2001 | 52AYY99KITCHEN AND TABLEWARE, N.E.C., (FOODWARE, COOKWARE & TABLEWARE) | 251POISONOUS | New Orleans District Office (NOL-DO) |
| 11/20/2001 | 52AIY32COFFEE/TEA POTS (FOODWARE, COOKWARE & TABLEWARE) | 238UNSAFE ADD | New Orleans District Office (NOL-DO) |
| 11/20/2001 | 52AIY28PLATES, ANY SIZE (FOODWARE, COOKWARE & TABLEWARE) | 238UNSAFE ADD | New Orleans District Office (NOL-DO) |
| 11/20/2001 | 52AIY31BOWLS, ANY SIZE (FOODWARE, COOKWARE & TABLEWARE) | 238UNSAFE ADD | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Faience Dap's FDA import refusal history?
Faience Dap (FEI: 3003461234) has 4 FDA import refusal record(s) in our database, spanning from 11/20/2001 to 11/20/2001.
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. Faience Dap's FEI number is 3003461234.
What types of violations has Faience Dap received?
Faience Dap 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 Faience Dap come from?
All FDA import refusal data for Faience Dap 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.