Dr. Taffi Srl
✅ Low Risk
FEI: 3005967802 • Osterode am Harz, Lower Saxony • GERMANY
FEI Number
3005967802
Location
Osterode am Harz, Lower Saxony
Country
GERMANYAddress
Dorgestr. 18-24, , Osterode am Harz, Lower Saxony, Germany
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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).
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
Refusal History
Frequently Asked Questions
What is Dr. Taffi Srl's FDA import refusal history?
Dr. Taffi Srl (FEI: 3005967802) has 1 FDA import refusal record(s) in our database, spanning from 11/28/2006 to 11/28/2006.
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. Dr. Taffi Srl's FEI number is 3005967802.
What types of violations has Dr. Taffi Srl received?
Dr. Taffi Srl 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 Dr. Taffi Srl come from?
All FDA import refusal data for Dr. Taffi Srl 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.