FDA Inspection 1196234 — Vascutek, Ltd.

Vascutek, Ltd. — FEI 3002808437

The FDA completed an inspection of Vascutek, Ltd. on Nov 17, 2022 in Inchinnan. 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: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 17, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Inchinnan (United Kingdom)

Additional details

Postmarket Audit Inspections

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