FDA Inspection 730088 — Mylan Laboratories Limited

Mylan Laboratories Limited — FEI 3005587313

The FDA completed an inspection of Mylan Laboratories Limited on May 27, 2011 in Sinnar. 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 27, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sinnar (India)