FDA Inspection 979499 — Aptuit (Oxford) Ltd.

Aptuit (Oxford) Ltd. — FEI 3003444315

The FDA completed an inspection of Aptuit (Oxford) Ltd. on July 22, 2016 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
July 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Abingdon (United Kingdom)