FDA Inspection 761720 — Alkem Laboratories Limited

Alkem Laboratories Limited — FEI 3006370524

The FDA completed an inspection of Alkem Laboratories Limited on December 9, 2011 in Daman. 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
December 9, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Daman (India)