Fiegert Enotech, Gmbh
⚠️ Moderate Risk
FEI: 3002961553 • Tuttlingen, Baden-Wurttemberg • GERMANY
FEI Number
3002961553
Location
Tuttlingen, Baden-Wurttemberg
Country
GERMANYAddress
D-78532, Gansacker 42, Tuttlingen, 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 |
|---|---|---|---|
| 7/22/2005 | 79HTDFORCEPS | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 7/22/2005 | 86HKBTELESCOPE, HAND-HELD, LOW-VISION | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 7/22/2005 | 79LRYPUNCH, SURGICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 7/22/2005 | 78FCLFORCEPS, BIOPSY, NON-ELECTRIC | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 7/22/2005 | 79LRWSCISSORS, GENERAL USE, SURGICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Fiegert Enotech, Gmbh's FDA import refusal history?
Fiegert Enotech, Gmbh (FEI: 3002961553) has 5 FDA import refusal record(s) in our database, spanning from 7/22/2005 to 7/22/2005.
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. Fiegert Enotech, Gmbh's FEI number is 3002961553.
What types of violations has Fiegert Enotech, Gmbh received?
Fiegert Enotech, Gmbh 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 Fiegert Enotech, Gmbh come from?
All FDA import refusal data for Fiegert Enotech, Gmbh 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.