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NewDeal SAS

⚠️ Moderate Risk

FEI: 3002952164 • Saint-Priest, Metropole de Lyon • FRANCE

FEI

FEI Number

3002952164

📍

Location

Saint-Priest, Metropole de Lyon

🇫🇷

Country

FRANCE
🏢

Address

Batiment Sequoia 2, 97 Allee Alexandre Borodine, Saint-Priest, Metropole de Lyon, France

Moderate Risk

FDA Import Risk Assessment

32.8
LowModerateHighCritical

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

Statistics

11
Total Refusals
4
Unique Violations
10/31/2019
Latest Refusal
6/9/2005
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
7.6×10%
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

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).

32809×

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.

3412×

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).

5082×

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.

Refusal History

DateProductViolationsDivision
10/31/2019
87HTYPIN, FIXATION, SMOOTH
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
79FZXGUIDE, SURGICAL, INSTRUMENT
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87HWCSCREW, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87HRSPLATE, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87HRSPLATE, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87HRSPLATE, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87HRSPLATE, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
10/31/2019
87HWCSCREW, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
6/9/2005
79HTZINSTRUMENT, CUTTING, ORTHOPEDIC
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
6/9/2005
87MOOORTHOPEDIC IMPLANT MATERIAL
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is NewDeal SAS's FDA import refusal history?

NewDeal SAS (FEI: 3002952164) has 11 FDA import refusal record(s) in our database, spanning from 6/9/2005 to 10/31/2019.

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. NewDeal SAS's FEI number is 3002952164.

What types of violations has NewDeal SAS received?

NewDeal SAS has been cited for 4 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 NewDeal SAS come from?

All FDA import refusal data for NewDeal 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.