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Chanel Products

⚠️ Moderate Risk

FEI: 3001891318 • Neuilly Sur Seine CEDEX, Hauts de Seine • FRANCE

FEI

FEI Number

3001891318

📍

Location

Neuilly Sur Seine CEDEX, Hauts de Seine

🇫🇷

Country

FRANCE
🏢

Address

Chanel, 135 avenue Charles de Gaulle, Neuilly Sur Seine CEDEX, Hauts de Seine, France

Moderate Risk

FDA Import Risk Assessment

42.5
LowModerateHighCritical

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

Statistics

32
Total Refusals
5
Unique Violations
6/18/2015
Latest Refusal
9/18/2004
Earliest Refusal

Score Breakdown

Violation Severity
56.6×40%
Refusal Volume
56.2×30%
Recency
0.0×20%
Frequency
29.8×10%
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

374112×

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.

7511×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

1189×

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).

2232×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

2351×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

Refusal History

DateProductViolationsDivision
6/18/2015
53GC03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
118NOT LISTED
Division of Southeast Imports (DSEI)
6/18/2015
53GC03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
118NOT LISTED
Division of Southeast Imports (DSEI)
9/25/2014
53GY03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
118NOT LISTED
Division of Southeast Imports (DSEI)
9/25/2014
53LC05HORMONE (SKIN CARE PREPARATIONS)
118NOT LISTED
Division of Southeast Imports (DSEI)
9/25/2014
53GH02FACE POWDERS (MAKEUP PREPARATIONS, NOT FOR EYES)
118NOT LISTED
Division of Southeast Imports (DSEI)
9/25/2014
53GH02FACE POWDERS (MAKEUP PREPARATIONS, NOT FOR EYES)
118NOT LISTED
Division of Southeast Imports (DSEI)
9/25/2014
53GY03FOUNDATIONS (MAKEUP PREPARATIONS, NOT FOR EYES)
118NOT LISTED
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
6/25/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
3741FRNMFGREG
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2013
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/20/2012
65LAY99PROTECTANT N.E.C.
118NOT LISTED
Division of Northeast Imports (DNEI)
10/1/2012
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
223FALSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/1/2012
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
223FALSE
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/26/2005
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
New Orleans District Office (NOL-DO)
9/18/2004
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Chanel Products's FDA import refusal history?

Chanel Products (FEI: 3001891318) has 32 FDA import refusal record(s) in our database, spanning from 9/18/2004 to 6/18/2015.

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. Chanel Products's FEI number is 3001891318.

What types of violations has Chanel Products received?

Chanel Products has been cited for 5 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 Chanel Products come from?

All FDA import refusal data for Chanel Products 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.