FDA Inspection 769752 — Vascutek, Ltd.

Vascutek, Ltd. — FEI 3002808437

The FDA completed an inspection of Vascutek, Ltd. on Feb 23, 2012 in Inchinnan. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Feb 23, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Inchinnan (United Kingdom)

Additional details

Postmarket Audit Inspections

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