L'Amy Incorporated
⚠️ Moderate Risk
FEI: 3000122956 • Wilton, CT • UNITED STATES
FEI Number
3000122956
Location
Wilton, CT
Country
UNITED STATESAddress
37 Danbury Rd, , Wilton, CT, United States
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 IMPACT
The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/21/2002 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | 235NOT IMPACT | New York District Office (NYK-DO) |
Frequently Asked Questions
What is L'Amy Incorporated's FDA import refusal history?
L'Amy Incorporated (FEI: 3000122956) has 1 FDA import refusal record(s) in our database, spanning from 5/21/2002 to 5/21/2002.
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. L'Amy Incorporated's FEI number is 3000122956.
What types of violations has L'Amy Incorporated received?
L'Amy Incorporated 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 L'Amy Incorporated come from?
All FDA import refusal data for L'Amy Incorporated 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.