Laboratorio Invermed
⚠️ Moderate Risk
FEI: 3007823194 • San Beranrdino • VENEZUELA
FEI Number
3007823194
Location
San Beranrdino
Country
VENEZUELAAddress
Av Erado Centro Profesional, , San Beranrdino, , Venezuela
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 Laboratorio Invermed's FDA import refusal history?
Laboratorio Invermed (FEI: 3007823194) has 2 FDA import refusal record(s) in our database, spanning from 8/19/2011 to 8/19/2011.
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. Laboratorio Invermed's FEI number is 3007823194.
What types of violations has Laboratorio Invermed received?
Laboratorio Invermed 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 Laboratorio Invermed come from?
All FDA import refusal data for Laboratorio Invermed 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.