Bayer OY
⚠️ Moderate Risk
FEI: 1000350927 • Turku, Varsinais-Suomi • FINLAND
FEI Number
1000350927
Location
Turku, Varsinais-Suomi
Country
FINLANDAddress
Pansiontie 47, , Turku, Varsinais-Suomi, Finland
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
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.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
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).
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/16/2022 | 65JCY36INTRAUTERINE COPPER (PROGESTIN) | 118NOT LISTED | Division of West Coast Imports (DWCI) |
| 6/17/2021 | 85HDTDEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER | Division of West Coast Imports (DWCI) | |
| 2/23/2021 | 85HDTDEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER | Division of West Coast Imports (DWCI) | |
| 2/2/2021 | 85HDTDEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER | Division of West Coast Imports (DWCI) | |
| 10/29/2013 | 64G29LEVONORGESTREL (ESTROGEN) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 10/24/2013 | 64GCC29LEVONORGESTREL (ESTROGEN) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 8/31/2011 | 65JCY36INTRAUTERINE COPPER (PROGESTIN) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Bayer OY's FDA import refusal history?
Bayer OY (FEI: 1000350927) has 7 FDA import refusal record(s) in our database, spanning from 8/31/2011 to 6/16/2022.
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. Bayer OY's FEI number is 1000350927.
What types of violations has Bayer OY received?
Bayer OY has been cited for 5 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 Bayer OY come from?
All FDA import refusal data for Bayer OY 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.