FDA Inspection 850564 — Jubilant Draximage Inc.

Jubilant Draximage Inc. — FEI 3009003838

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

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