Fp Company
⚠️ Moderate Risk
FEI: 3010684892 • Paris, Paris • FRANCE
FEI Number
3010684892
Location
Paris, Paris
Country
FRANCEAddress
42 Quai De Jemmapes, , Paris, Paris, 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).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/15/2022 | 85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE | Division of Southeast Imports (DSEI) | |
| 12/19/2017 | 85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE | Division of Northern Border Imports (DNBI) | |
| 4/30/2014 | 53TH99COSMETIC PRODUCTS CONTAINING ANIMAL BY-PRODUCTS (PORCINE), N.E.C. | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 4/30/2014 | 97RALMASSAGER, ULTRASONIC NON-MEDICAL DEVICES | 16DIRECTIONS | Division of Southeast Imports (DSEI) |
| 4/30/2014 | 97RALMASSAGER, ULTRASONIC NON-MEDICAL DEVICES | 16DIRECTIONS | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Fp Company's FDA import refusal history?
Fp Company (FEI: 3010684892) has 5 FDA import refusal record(s) in our database, spanning from 4/30/2014 to 9/15/2022.
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. Fp Company's FEI number is 3010684892.
What types of violations has Fp Company received?
Fp Company has been cited for 6 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 Fp Company come from?
All FDA import refusal data for Fp Company 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.