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LENS COM.DE ARTIGOS OPTICOS LTDA

⚠️ Moderate Risk

FEI: 3013430742 • Curitiba • BRAZIL

FEI

FEI Number

3013430742

📍

Location

Curitiba

🇧🇷

Country

BRAZIL
🏢

Address

Rua des Aurelio Feijo 1, , Curitiba, , Brazil

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

7
Total Refusals
6
Unique Violations
7/7/2017
Latest Refusal
6/26/2017
Earliest Refusal

Score Breakdown

Violation Severity
54.2×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

1187×

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).

167×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

32607×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

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.

847×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

2231×

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.

Refusal History

DateProductViolationsDivision
7/7/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
223FALSE
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)
6/30/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)
6/30/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)
6/30/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)
6/30/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)
6/30/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)
6/26/2017
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
16DIRECTIONS
3260NO ENGLISH
3280FRNMFGREG
84RX DEVICE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LENS COM.DE ARTIGOS OPTICOS LTDA's FDA import refusal history?

LENS COM.DE ARTIGOS OPTICOS LTDA (FEI: 3013430742) has 7 FDA import refusal record(s) in our database, spanning from 6/26/2017 to 7/7/2017.

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. LENS COM.DE ARTIGOS OPTICOS LTDA's FEI number is 3013430742.

What types of violations has LENS COM.DE ARTIGOS OPTICOS LTDA received?

LENS COM.DE ARTIGOS OPTICOS LTDA has been cited for 6 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 LENS COM.DE ARTIGOS OPTICOS LTDA come from?

All FDA import refusal data for LENS COM.DE ARTIGOS OPTICOS LTDA 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.