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II-VI LASER ENTERPRISE PHILIPPIN

⚠️ High Risk

FEI: 3015250017 • Calamba City • PHILIPPINES

FEI

FEI Number

3015250017

📍

Location

Calamba City

🇵🇭
🏢

Address

Bldg. 5, Ezp Center, , Calamba City, , Philippines

High Risk

FDA Import Risk Assessment

53.2
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
1/12/2026
Latest Refusal
1/12/2026
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
97.4×20%
Frequency
30.0×10%
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

4763×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
1/12/2026
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of West Coast Imports (DWCI)
1/12/2026
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of West Coast Imports (DWCI)
1/12/2026
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is II-VI LASER ENTERPRISE PHILIPPIN's FDA import refusal history?

II-VI LASER ENTERPRISE PHILIPPIN (FEI: 3015250017) has 3 FDA import refusal record(s) in our database, spanning from 1/12/2026 to 1/12/2026.

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. II-VI LASER ENTERPRISE PHILIPPIN's FEI number is 3015250017.

What types of violations has II-VI LASER ENTERPRISE PHILIPPIN received?

II-VI LASER ENTERPRISE PHILIPPIN 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 II-VI LASER ENTERPRISE PHILIPPIN come from?

All FDA import refusal data for II-VI LASER ENTERPRISE PHILIPPIN 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.