FDA Inspection 1030430 — BWXT Medical Ltd

BWXT Medical Ltd — FEI 3004005970

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.