Pab
⚠️ Moderate Risk
FEI: 3003613398 • Bondoufle, Essonne • FRANCE
FEI Number
3003613398
Location
Bondoufle, Essonne
Country
FRANCEAddress
2 Rue Pierre Josse, , Bondoufle, Essonne, 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
POISONOUS
The article is subject to refusal of admission pursuant Section 801(a)(3) in that The cosmetic appears to bear or contain a poisonous or deleterious substance which may render it injurious to users under the conditions prescribed in the labeling thereof, or, under such conditions of use as are customary or usual.
FILTH
The cosmetic appears to consist in whole or in part of any filthy, putrid, or decomposed substance.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/22/2004 | 53LD99OTHER SKIN CARE PREPARATIONS, N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 12/22/2004 | 53LD99OTHER SKIN CARE PREPARATIONS, N.E.C. | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 6/8/2004 | 53PD02COLLAGEN (COSMETIC RAW MATERIAL) | 312FILTH | Los Angeles District Office (LOS-DO) |
| 6/8/2004 | 53PD02COLLAGEN (COSMETIC RAW MATERIAL) | 310POISONOUS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Pab's FDA import refusal history?
Pab (FEI: 3003613398) has 4 FDA import refusal record(s) in our database, spanning from 6/8/2004 to 12/22/2004.
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. Pab's FEI number is 3003613398.
What types of violations has Pab received?
Pab has been cited for 3 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 Pab come from?
All FDA import refusal data for Pab 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.