FDA Inspection 915098 — KDC/One Swallowfield Limited

KDC/One Swallowfield Limited — FEI 3005246013

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

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