Workshop Conferences
⚠️ Moderate Risk
FEI: 3006319430 • Loughborough, FN • UNITED KINGDOM
FEI Number
3006319430
Location
Loughborough, FN
Country
UNITED KINGDOMAddress
105 Ashby Rd, , Loughborough, FN, United Kingdom
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
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/26/2007 | 79GALSUTURE, ABSORBABLE, NATURAL | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 90LXEDOPPLER, FETAL, ULTRASOUND | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 79HTCPLIERS, SURGICAL | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 79LRWSCISSORS, GENERAL USE, SURGICAL | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 86HLIOPHTHALMOSCOPE, AC-POWERED | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 86HJQSTEREOSCOPE, AC-POWERED | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 79HAYSPONGE (EXTERNAL USE) | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 80BYYTUBE, ASPIRATING, FLEXIBLE, CONNECTING | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 74DQFACTUATOR, SYRINGE, INJECTOR TYPE | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 79GAANEEDLE, ASPIRATION AND INJECTION, DISPOSABLE | 341REGISTERED | Baltimore District Office (BLT-DO) |
| 6/26/2007 | 74DPSELECTROCARDIOGRAPH | 341REGISTERED | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Workshop Conferences's FDA import refusal history?
Workshop Conferences (FEI: 3006319430) has 11 FDA import refusal record(s) in our database, spanning from 6/26/2007 to 6/26/2007.
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. Workshop Conferences's FEI number is 3006319430.
What types of violations has Workshop Conferences received?
Workshop Conferences 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 Workshop Conferences come from?
All FDA import refusal data for Workshop Conferences 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.