VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI
⚠️ Moderate Risk
FEI: 3015512211 • Sariyer, Sariyer Istanbul • TURKEY
FEI Number
3015512211
Location
Sariyer, Sariyer Istanbul
Country
TURKEYAddress
Teknokent Ari 1 Sit. No: 2 5 15, , Sariyer, Sariyer Istanbul, Turkey
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/3/2024 | 80PWCGENERAL WELLNESS PRODUCT | 508NO 510(K) | Division of Northeast Imports (DNEI) |
| 6/3/2022 | 75LXGEQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 4/20/2022 | 75LXGEQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 9/9/2019 | 75LXGEQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI's FDA import refusal history?
VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI (FEI: 3015512211) has 4 FDA import refusal record(s) in our database, spanning from 9/9/2019 to 4/3/2024.
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. VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI's FEI number is 3015512211.
What types of violations has VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI received?
VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI has been cited for 3 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 VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI come from?
All FDA import refusal data for VIVOSENS BIYOTEKNOLOJI AR-GE, SAN. & TIC. LTD. STI 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.