Drogueria Luipharm
✅ Low Risk
FEI: 3010975322 • Guatemala City • GUATEMALA
FEI Number
3010975322
Location
Guatemala City
Country
GUATEMALAAddress
6 Calle 3212 Km 155 Zona 6, , Guatemala City, , Guatemala
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
Frequently Asked Questions
What is Drogueria Luipharm's FDA import refusal history?
Drogueria Luipharm (FEI: 3010975322) has 1 FDA import refusal record(s) in our database, spanning from 10/6/2015 to 10/6/2015.
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. Drogueria Luipharm's FEI number is 3010975322.
What types of violations has Drogueria Luipharm received?
Drogueria Luipharm has been cited for 2 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 Drogueria Luipharm come from?
All FDA import refusal data for Drogueria Luipharm 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.