FDA Inspection 979499 — Aptuit (Oxford) Ltd.

Aptuit (Oxford) Ltd. — FEI 3003444315

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

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