Protrans Med Diag
⚠️ Moderate Risk
FEI: 3006313869 • Hockenheim, Baden-Wurttemberg • GERMANY
FEI Number
3006313869
Location
Hockenheim, Baden-Wurttemberg
Country
GERMANYAddress
Ketschau 2, , Hockenheim, Baden-Wurttemberg, Germany
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/24/2007 | 83JTODISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 8/24/2007 | 83JTODISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 8/24/2007 | 83MWASYSTEM, NUCLEIC ACID AMPLIFICATION, MYCOBACTERIUM TUBERCULOSIS COMPLEX | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 8/24/2007 | 83JTODISCS, STRIPS AND REAGENTS, MICROORGANISM DIFFERENTIATION | 118NOT LISTED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Protrans Med Diag's FDA import refusal history?
Protrans Med Diag (FEI: 3006313869) has 4 FDA import refusal record(s) in our database, spanning from 8/24/2007 to 8/24/2007.
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. Protrans Med Diag's FEI number is 3006313869.
What types of violations has Protrans Med Diag received?
Protrans Med Diag has been cited for 1 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 Protrans Med Diag come from?
All FDA import refusal data for Protrans Med Diag 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.