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R C S Comercio De Artigos Opt

⚠️ Moderate Risk

FEI: 3011588869 • Curitiba, Parana • BRAZIL

FEI

FEI Number

3011588869

📍

Location

Curitiba, Parana

🇧🇷

Country

BRAZIL
🏢

Address

Avenida Parana 33 Cj 32 ESala 25, , Curitiba, Parana, Brazil

Moderate Risk

FDA Import Risk Assessment

40.9
LowModerateHighCritical

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

Statistics

8
Total Refusals
4
Unique Violations
7/20/2015
Latest Refusal
7/17/2015
Earliest Refusal

Score Breakdown

Violation Severity
55.8×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
80.0×10%
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

1188×

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).

5088×

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.

32807×

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.

3411×

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).

Refusal History

DateProductViolationsDivision
7/20/2015
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/20/2015
86LPMLENSES, SOFT CONTACT, EXTENDED WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/17/2015
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/17/2015
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/17/2015
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/17/2015
86MVNLENS, CONTACT (DISPOSABLE)
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/17/2015
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/17/2015
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
118NOT LISTED
341REGISTERED
508NO 510(K)
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is R C S Comercio De Artigos Opt's FDA import refusal history?

R C S Comercio De Artigos Opt (FEI: 3011588869) has 8 FDA import refusal record(s) in our database, spanning from 7/17/2015 to 7/20/2015.

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. R C S Comercio De Artigos Opt's FEI number is 3011588869.

What types of violations has R C S Comercio De Artigos Opt received?

R C S Comercio De Artigos Opt 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 R C S Comercio De Artigos Opt come from?

All FDA import refusal data for R C S Comercio De Artigos Opt 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.