RITM OKB ZAO
⚠️ Moderate Risk
FEI: 3007028037 • Taganrog, Rostovskaya obl • RUSSIA
FEI Number
3007028037
Location
Taganrog, Rostovskaya obl
Country
RUSSIAAddress
Ul. Petrovskaya 99, , Taganrog, Rostovskaya obl, Russia
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/11/2011 | 84HCCDEVICE, BIOFEEDBACK | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 1/11/2011 | 84HCCDEVICE, BIOFEEDBACK | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 1/11/2011 | 84HCCDEVICE, BIOFEEDBACK | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 1/11/2011 | 84HCCDEVICE, BIOFEEDBACK | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 1/11/2011 | 84HCCDEVICE, BIOFEEDBACK | 508NO 510(K) | Southwest Import District Office (SWI-DO) |
| 10/17/2008 | 84NHINERVE, STIMULATOR, ELECTRICAL, PERCUTANEOUS (PENS) FOR PAIN RELIEF | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is RITM OKB ZAO's FDA import refusal history?
RITM OKB ZAO (FEI: 3007028037) has 6 FDA import refusal record(s) in our database, spanning from 10/17/2008 to 1/11/2011.
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. RITM OKB ZAO's FEI number is 3007028037.
What types of violations has RITM OKB ZAO received?
RITM OKB ZAO 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 RITM OKB ZAO come from?
All FDA import refusal data for RITM OKB ZAO 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.