FDA Inspection 763938 — Sipra Labs Limited

Sipra Labs Limited — FEI 3004544153

The FDA completed an inspection of Sipra Labs Limited on September 22, 2011 in Hyderabad. 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
September 22, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hyderabad (India)