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PEGAVISION CORPORATION

⚠️ High Risk

FEI: 3021516371 • Dashi • TAIWAN

FEI

FEI Number

3021516371

📍

Location

Dashi

🇹🇼

Country

TAIWAN
🏢

Address

No 255 Sec 2 Renhe Rd, , Dashi, , Taiwan

High Risk

FDA Import Risk Assessment

58.9
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
10/22/2025
Latest Refusal
10/22/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
25.9×30%
Recency
95.6×20%
Frequency
40.0×10%
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

844×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
10/22/2025
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
84RX DEVICE
Division of Southeast Imports (DSEI)
10/22/2025
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
84RX DEVICE
Division of Southeast Imports (DSEI)
10/22/2025
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
84RX DEVICE
Division of Southeast Imports (DSEI)
10/22/2025
86HQDLENS, CONTACT (OTHER MATERIAL) - DAILY
84RX DEVICE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PEGAVISION CORPORATION's FDA import refusal history?

PEGAVISION CORPORATION (FEI: 3021516371) has 4 FDA import refusal record(s) in our database, spanning from 10/22/2025 to 10/22/2025.

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. PEGAVISION CORPORATION's FEI number is 3021516371.

What types of violations has PEGAVISION CORPORATION received?

PEGAVISION CORPORATION 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 PEGAVISION CORPORATION come from?

All FDA import refusal data for PEGAVISION CORPORATION 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.