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FDA Inspection 839012 — Mylan Laboratories Limited

Mylan Laboratories Limited — FEI 3007648351

The FDA completed an inspection of Mylan Laboratories Limited on June 27, 2013 in Bengaluru. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 27, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bengaluru (India)

Facility

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  • 1119165 (VAI Fri Feb 28 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1089838 (VAI Mon May 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1017161 (VAI Tue Apr 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 966686 (VAI Wed Apr 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources