FDA Inspection 1275545 — Douglas Manufacturing Limited

Douglas Manufacturing Limited — FEI 3005641565

The FDA completed an inspection of Douglas Manufacturing Limited on May 30, 2025 in Auckland. 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
May 30, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Auckland (New Zealand)

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