FDA Inspection 963420 — OneSource Specialty Pharma Limited

OneSource Specialty Pharma Limited — FEI 3003813519

The FDA completed an inspection of OneSource Specialty Pharma Limited on Mar 16, 2016 in Bengaluru. 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 16, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bengaluru (India)

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