FDA Inspection 827247 — Jubilant DraxImage Radiopharmacies

Jubilant DraxImage Radiopharmacies — FEI 3006563584

The FDA completed an inspection of Jubilant DraxImage Radiopharmacies on April 12, 2013 in Mobile, AL. 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
April 12, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mobile, AL (United States)