Liko North America, Subsidiary Of Hill-rom, Inc. – FDA Inspection, Sep 24, 2010

Record Details

This FDA Inspection record concerns Liko North America, Subsidiary Of Hill-rom, Inc., with an inspection on September 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Liko North America, Subsidiary Of Hill-rom, Inc.
Inspection Date: September 24, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6a13da05-5c9a-4d2f-8e7b-3b55bb37dace

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 682329
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices

FDA Citations

21 CFR 803.50(a)(2)Individual Report of Malfunction

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FDA Inspection

Liko North America, Subsidiary Of Hill-rom, Inc.September 24, 2010