TODA PHARMA
⚠️ Moderate Risk
FEI: 3016688289 • Strasbourg, Bas Rhin • FRANCE
FEI Number
3016688289
Location
Strasbourg, Bas Rhin
Country
FRANCEAddress
2 Rue Du Rhin Napoleon, , Strasbourg, Bas Rhin, France
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 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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/28/2021 | 83QMNCOVID-19 MULTI-ANALYTE ANTIGEN DEVICE | 237NO PMA | Division of Southwest Imports (DSWI) |
| 4/28/2021 | 83QMNCOVID-19 MULTI-ANALYTE ANTIGEN DEVICE | 237NO PMA | Division of Southwest Imports (DSWI) |
| 12/29/2020 | 83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM. | 508NO 510(K) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is TODA PHARMA's FDA import refusal history?
TODA PHARMA (FEI: 3016688289) has 3 FDA import refusal record(s) in our database, spanning from 12/29/2020 to 4/28/2021.
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. TODA PHARMA's FEI number is 3016688289.
What types of violations has TODA PHARMA received?
TODA PHARMA 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 TODA PHARMA come from?
All FDA import refusal data for TODA PHARMA 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.