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AMHERST LABS INC

⚠️ High Risk

FEI: 3012620079 • Laguna • PHILIPPINES

FEI

FEI Number

3012620079

📍

Location

Laguna

🇵🇭
🏢

Address

Unilab Pharma Campus Br, , Laguna, , Philippines

High Risk

FDA Import Risk Assessment

53.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
6/13/2024
Latest Refusal
12/18/2017
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
53.6×20%
Frequency
4.6×10%
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

753×

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
6/13/2024
62OCA14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/13/2024
61PCA99ANTI-DIABETIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/18/2017
60XCB17ATENOLOL (ANTI-ADRENERGIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AMHERST LABS INC's FDA import refusal history?

AMHERST LABS INC (FEI: 3012620079) has 3 FDA import refusal record(s) in our database, spanning from 12/18/2017 to 6/13/2024.

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. AMHERST LABS INC's FEI number is 3012620079.

What types of violations has AMHERST LABS INC received?

AMHERST LABS INC 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 AMHERST LABS INC come from?

All FDA import refusal data for AMHERST LABS INC 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.