FDA Inspection 847980 — Aptuit (Oxford) Ltd.

Aptuit (Oxford) Ltd. — FEI 3003444315

The FDA completed an inspection of Aptuit (Oxford) Ltd. on September 13, 2013 in Abingdon. 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
September 13, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Abingdon (United Kingdom)