FDA Inspection 1110387 — Douglas Manufacturing Limited

Douglas Manufacturing Limited — FEI 3005641565

The FDA completed an inspection of Douglas Manufacturing Limited on October 11, 2019 in Auckland. 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
October 11, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Auckland (New Zealand)