FDA Inspection 711567 — Apotex Pharmachem India Pvt Ltd.

Apotex Pharmachem India Pvt Ltd. — FEI 3005466325

The FDA completed an inspection of Apotex Pharmachem India Pvt Ltd. on Dec 1, 2010 in Bangalore. 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 1, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bangalore (India)

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