ARMSTRONG LABORATORIES OF MEXICO
⚠️ High Risk
FEI: 3016682508 • Iztapalapa • MEXICO
FEI Number
3016682508
Location
Iztapalapa
Country
MEXICOAddress
Anillo Periferico No 23, , Iztapalapa, , Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
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 ARMSTRONG LABORATORIES OF MEXICO's FDA import refusal history?
ARMSTRONG LABORATORIES OF MEXICO (FEI: 3016682508) has 2 FDA import refusal record(s) in our database, spanning from 2/28/2022 to 12/9/2025.
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. ARMSTRONG LABORATORIES OF MEXICO's FEI number is 3016682508.
What types of violations has ARMSTRONG LABORATORIES OF MEXICO received?
ARMSTRONG LABORATORIES OF MEXICO 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 ARMSTRONG LABORATORIES OF MEXICO come from?
All FDA import refusal data for ARMSTRONG LABORATORIES OF MEXICO 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.