FDA Inspection 954842 — Centrient Pharmaceuticals India Private Limited

Centrient Pharmaceuticals India Private Limited — FEI 3004497364

The FDA completed an inspection of Centrient Pharmaceuticals India Private Limited on Dec 18, 2015 in Nawashahr. 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
Dec 18, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nawashahr (India)

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