Fr Fassmer Gmbh & Co.
⚠️ Moderate Risk
FEI: 3008338587 • Berne • 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
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/14/2011 | 95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS | 126FAILS STD | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Fr Fassmer Gmbh & Co.'s FDA import refusal history?
Fr Fassmer Gmbh & Co. (FEI: 3008338587) has 1 FDA import refusal record(s) in our database, spanning from 6/14/2011 to 6/14/2011.
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. Fr Fassmer Gmbh & Co.'s FEI number is 3008338587.
What types of violations has Fr Fassmer Gmbh & Co. received?
Fr Fassmer Gmbh & Co. 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 Fr Fassmer Gmbh & Co. come from?
All FDA import refusal data for Fr Fassmer Gmbh & Co. 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.