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ARMSTRONG LABORATIOS DE MEXICO

⚠️ Moderate Risk

FEI: 3013292313 • Ciudad De Mexico, Ciudad de Mexico • MEXICO

FEI

FEI Number

3013292313

📍

Location

Ciudad De Mexico, Ciudad de Mexico

🇲🇽

Country

MEXICO
🏢

Address

Av Division Del Norte 3, Col. Belisario Dominguez, Tlalpan, Ciudad De Mexico, Ciudad de Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

49.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
1
Unique Violations
8/23/2023
Latest Refusal
3/31/2017
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
37.0×20%
Frequency
3.1×10%
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

752×

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

DateProductViolationsDivision
8/23/2023
65RDA14POTASSIUM CHLORIDE (REPLENISHER)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/31/2017
62ODY24DILTIAZEM HYDROCHLORIDE (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ARMSTRONG LABORATIOS DE MEXICO's FDA import refusal history?

ARMSTRONG LABORATIOS DE MEXICO (FEI: 3013292313) has 2 FDA import refusal record(s) in our database, spanning from 3/31/2017 to 8/23/2023.

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 LABORATIOS DE MEXICO's FEI number is 3013292313.

What types of violations has ARMSTRONG LABORATIOS DE MEXICO received?

ARMSTRONG LABORATIOS DE 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 LABORATIOS DE MEXICO come from?

All FDA import refusal data for ARMSTRONG LABORATIOS DE 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.