FDA Inspection 960871 — Mylan Laboratories Limited

Mylan Laboratories Limited — FEI 3010453141

The FDA completed an inspection of Mylan Laboratories Limited on February 5, 2016 in Pithampur, District Dhar. 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
February 5, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pithampur, District Dhar (India)