FDA Inspection 648411 — Zentiva Private Limited

Zentiva Private Limited — FEI 3004086396

The FDA completed an inspection of Zentiva Private Limited on Sep 4, 2009 in Ankleshwar. 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
Sep 4, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ankleshwar (India)

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