FDA Inspection 1030430 — BWXT Medical Ltd

BWXT Medical Ltd — FEI 3004005970

The FDA completed an inspection of BWXT Medical Ltd on September 22, 2017 in Vancouver. 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, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vancouver (Canada)