LABORATORY LANCASCO
⚠️ Moderate Risk
FEI: 3013755052 • Guatemala City • GUATEMALA
FEI Number
3013755052
Location
Guatemala City
Country
GUATEMALAAddress
Calzada Aguilar Batres, , Guatemala City, , Guatemala
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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
Frequently Asked Questions
What is LABORATORY LANCASCO's FDA import refusal history?
LABORATORY LANCASCO (FEI: 3013755052) has 2 FDA import refusal record(s) in our database, spanning from 10/11/2017 to 10/11/2017.
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. LABORATORY LANCASCO's FEI number is 3013755052.
What types of violations has LABORATORY LANCASCO received?
LABORATORY LANCASCO 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 LABORATORY LANCASCO come from?
All FDA import refusal data for LABORATORY LANCASCO 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.