FDA Inspection 1007598 — Alkem Laboratories Limited

Alkem Laboratories Limited — FEI 3006370533

The FDA completed an inspection of Alkem Laboratories Limited on Mar 10, 2017 in Tehsil Nalagarh, Baddi. 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
Mar 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tehsil Nalagarh, Baddi (India)

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