FDA Inspection 711776 — Mylan Laboratories Limited

Mylan Laboratories Limited — FEI 3007512701

The FDA completed an inspection of Mylan Laboratories Limited on January 25, 2011 in Anekal Taluk, Bangalore. 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
January 25, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anekal Taluk, Bangalore (India)