FDA Inspection 1166008 — KDC/One Swallowfield Limited

KDC/One Swallowfield Limited — FEI 3005246013

The FDA completed an inspection of KDC/One Swallowfield Limited on April 14, 2021 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
April 14, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wellington (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)