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 Nashik. 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
May 27, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nashik (India)

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