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Face A Face Architectures

⚠️ Moderate Risk

FEI: 3003261430 • Paris, Paris • FRANCE

FEI

FEI Number

3003261430

📍

Location

Paris, Paris

🇫🇷

Country

FRANCE
🏢

Address

189 Rue D Aubervilliers, , Paris, Paris, France

Moderate Risk

FDA Import Risk Assessment

34.2
LowModerateHighCritical

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

Statistics

23
Total Refusals
5
Unique Violations
8/23/2013
Latest Refusal
5/15/2003
Earliest Refusal

Score Breakdown

Violation Severity
41.6×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
22.4×10%
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

34113×

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).

11812×

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).

32803×

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.

2352×

NOT IMPACT

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

37411×

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
8/23/2013
86HQZFRAME, SPECTACLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
New Orleans District Office (NOL-DO)
8/23/2013
86HQZFRAME, SPECTACLE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
New Orleans District Office (NOL-DO)
8/23/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
1/4/2013
86HQZFRAME, SPECTACLE
341REGISTERED
Detroit District Office (DET-DO)
1/4/2013
86HQZFRAME, SPECTACLE
341REGISTERED
Detroit District Office (DET-DO)
1/4/2013
86HQZFRAME, SPECTACLE
341REGISTERED
Detroit District Office (DET-DO)
1/2/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
341REGISTERED
Detroit District Office (DET-DO)
1/2/2013
86HQZFRAME, SPECTACLE
341REGISTERED
Detroit District Office (DET-DO)
1/2/2013
86HQZFRAME, SPECTACLE
341REGISTERED
Detroit District Office (DET-DO)
10/28/2011
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)
10/28/2011
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)
10/28/2011
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)
10/8/2010
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)
10/8/2010
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
New Orleans District Office (NOL-DO)
10/8/2010
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)
5/20/2009
86HQZFRAME, SPECTACLE
341REGISTERED
New York District Office (NYK-DO)
5/20/2009
86HQZFRAME, SPECTACLE
341REGISTERED
New York District Office (NYK-DO)
5/20/2009
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
341REGISTERED
New York District Office (NYK-DO)
5/15/2003
86HQZFRAME, SPECTACLE
341REGISTERED
New Orleans District Office (NOL-DO)
5/15/2003
86HQZFRAME, SPECTACLE
341REGISTERED
New Orleans District Office (NOL-DO)
5/15/2003
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
New Orleans District Office (NOL-DO)
5/15/2003
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)
5/15/2003
86HQZFRAME, SPECTACLE
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Face A Face Architectures's FDA import refusal history?

Face A Face Architectures (FEI: 3003261430) has 23 FDA import refusal record(s) in our database, spanning from 5/15/2003 to 8/23/2013.

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. Face A Face Architectures's FEI number is 3003261430.

What types of violations has Face A Face Architectures received?

Face A Face Architectures 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 Face A Face Architectures come from?

All FDA import refusal data for Face A Face Architectures 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.