Shoppers Drug Mart
⚠️ Moderate Risk
FEI: 1000333799 • Charlottetown, Prince Edward Island • CANADA
FEI Number
1000333799
Location
Charlottetown, Prince Edward Island
Country
CANADAAddress
390 University Ave, , Charlottetown, Prince Edward Island, Canada
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
AGR RX
The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.
Refusal History
Frequently Asked Questions
What is Shoppers Drug Mart's FDA import refusal history?
Shoppers Drug Mart (FEI: 1000333799) has 2 FDA import refusal record(s) in our database, spanning from 1/3/2002 to 1/3/2002.
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. Shoppers Drug Mart's FEI number is 1000333799.
What types of violations has Shoppers Drug Mart received?
Shoppers Drug Mart 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 Shoppers Drug Mart come from?
All FDA import refusal data for Shoppers Drug Mart 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.