FDA Inspection 915098 — KDC/One Swallowfield Limited

KDC/One Swallowfield Limited — FEI 3005246013

The FDA completed an inspection of KDC/One Swallowfield Limited on January 30, 2015 in Wellington. 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
January 30, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wellington (United Kingdom)