FDA Inspection 1098898 — Aptuit (Oxford) Ltd.

Aptuit (Oxford) Ltd. — FEI 3003444315

The FDA completed an inspection of Aptuit (Oxford) Ltd. on November 16, 2018 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
November 16, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Abingdon (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)