FDA Inspection 939758 — Mylan Laboratories Limited

Mylan Laboratories Limited — FEI 3008725991

The FDA completed an inspection of Mylan Laboratories Limited on Jul 24, 2015 in Valsad District. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 24, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Valsad District (India)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.