FDA Inspection 850564 — Jubilant Draximage Inc.

Jubilant Draximage Inc. — FEI 3009003838

The FDA completed an inspection of Jubilant Draximage Inc. on September 17, 2013 in Kirkland. 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 17, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kirkland (Canada)