FDA Inspection 635196 — Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited)

Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited) — FEI 3005674618

The FDA completed an inspection of Vitalife Laboratories (A Div. Of Arch Pharmalabs Limited) on November 20, 2009 in Gurugram. 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
November 20, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gurugram (India)