FDA Inspection 797064 — Huntleigh Healthcare Ltd.

Huntleigh Healthcare Ltd. — FEI 1000589001

The FDA completed an inspection of Huntleigh Healthcare Ltd. on Sep 6, 2012 in Cardiff. 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
Sep 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Cardiff (United Kingdom)

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