FDA Inspection 1237801 — Mylan Laboratories Limited

Mylan Laboratories Limited — FEI 3008255419

The FDA completed an inspection of Mylan Laboratories Limited on May 17, 2024 in Hosur. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 17, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hosur (India)