FDA Inspection 1292500 — Mylan, Inc. A Viatris Company

Mylan, Inc. A Viatris Company — FEI 3042120103

The FDA completed an inspection of Mylan, Inc. A Viatris Company on December 12, 2025 in Canonsburg, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 12, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Canonsburg, PA (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
745221 CFR 312.56(c)IND safety report