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MYLAN SPECIAL PRODUCT LINE SPA

⚠️ High Risk

FEI: 3020939582 • Anagni • ITALY

FEI

FEI Number

3020939582

📍

Location

Anagni

🇮🇹

Country

ITALY
🏢

Address

Via Fratta Rotonda Vadl, , Anagni, , Italy

High Risk

FDA Import Risk Assessment

57.8
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
5/28/2025
Latest Refusal
2/5/2025
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
72.6×20%
Frequency
20.0×10%
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

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
5/28/2025
64MDA01CLOMIPHENE CITRATE (GONAD-STIMULATING PRINCIPLE)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/5/2025
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MYLAN SPECIAL PRODUCT LINE SPA's FDA import refusal history?

MYLAN SPECIAL PRODUCT LINE SPA (FEI: 3020939582) has 2 FDA import refusal record(s) in our database, spanning from 2/5/2025 to 5/28/2025.

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. MYLAN SPECIAL PRODUCT LINE SPA's FEI number is 3020939582.

What types of violations has MYLAN SPECIAL PRODUCT LINE SPA received?

MYLAN SPECIAL PRODUCT LINE SPA 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 MYLAN SPECIAL PRODUCT LINE SPA come from?

All FDA import refusal data for MYLAN SPECIAL PRODUCT LINE SPA 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.