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Caudalie Sas

⚠️ Moderate Risk

FEI: 3009801620 • St Jean de Braye, Loiret • FRANCE

FEI

FEI Number

3009801620

📍

Location

St Jean de Braye, Loiret

🇫🇷

Country

FRANCE
🏢

Address

9 Boulevard De La Salle, , St Jean de Braye, Loiret, France

Moderate Risk

FDA Import Risk Assessment

40.4
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

10
Total Refusals
3
Unique Violations
3/11/2014
Latest Refusal
9/27/2013
Earliest Refusal

Score Breakdown

Violation Severity
47.1×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11810×

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).

32802×

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.

37412×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

Refusal History

DateProductViolationsDivision
3/11/2014
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
3/11/2014
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
3/11/2014
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
3/11/2014
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
3/11/2014
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
3/11/2014
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
10/22/2013
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
10/22/2013
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
9/27/2013
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
Division of Northeast Imports (DNEI)
9/27/2013
66PDL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Caudalie Sas's FDA import refusal history?

Caudalie Sas (FEI: 3009801620) has 10 FDA import refusal record(s) in our database, spanning from 9/27/2013 to 3/11/2014.

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. Caudalie Sas's FEI number is 3009801620.

What types of violations has Caudalie Sas received?

Caudalie Sas 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 Caudalie Sas come from?

All FDA import refusal data for Caudalie Sas 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.