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FIBROBETON YAPI ELEMANLARI

Low Risk

FEI: 3019689394 • Kavacik • TURKEY

FEI

FEI Number

3019689394

📍

Location

Kavacik

🇹🇷

Country

TURKEY
🏢

Address

San Ins Ve Tic A.S., Er, , Kavacik, , Turkey

Low Risk

FDA Import Risk Assessment

24.5
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
10/11/2022
Latest Refusal
10/11/2022
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
20.9×20%
Frequency
10.0×10%
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

1181×

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).

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
10/11/2022
80QLADECONTAMINATION SYSTEMS FOR FACEMASKS, SURGICAL MASKS, FACE SHIELDS, AND SAFETY GLASSES
118NOT LISTED
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is FIBROBETON YAPI ELEMANLARI's FDA import refusal history?

FIBROBETON YAPI ELEMANLARI (FEI: 3019689394) has 1 FDA import refusal record(s) in our database, spanning from 10/11/2022 to 10/11/2022.

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. FIBROBETON YAPI ELEMANLARI's FEI number is 3019689394.

What types of violations has FIBROBETON YAPI ELEMANLARI received?

FIBROBETON YAPI ELEMANLARI 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 FIBROBETON YAPI ELEMANLARI come from?

All FDA import refusal data for FIBROBETON YAPI ELEMANLARI 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.