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Apro Srl

⚠️ Moderate Risk

FEI: 3011916677 • Giugliano In Ca • ITALY

FEI

FEI Number

3011916677

📍

Location

Giugliano In Ca

🇮🇹

Country

ITALY
🏢

Address

Via Carla Botta 1, , Giugliano In Ca, , Italy

Moderate Risk

FDA Import Risk Assessment

38.0
LowModerateHighCritical

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

Statistics

11
Total Refusals
2
Unique Violations
6/13/2019
Latest Refusal
6/13/2019
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
100.0×10%
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

328011×

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.

34111×

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
6/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQZFRAME, SPECTACLE
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQZFRAME, SPECTACLE
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQZFRAME, SPECTACLE
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQZFRAME, SPECTACLE
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
6/13/2019
86HQZFRAME, SPECTACLE
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Apro Srl's FDA import refusal history?

Apro Srl (FEI: 3011916677) has 11 FDA import refusal record(s) in our database, spanning from 6/13/2019 to 6/13/2019.

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. Apro Srl's FEI number is 3011916677.

What types of violations has Apro Srl received?

Apro Srl has been cited for 2 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 Apro Srl come from?

All FDA import refusal data for Apro Srl 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.