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 December 1, 2010 in Bangalore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 1, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bangalore (India)