Biomet U.K., Ltd. – FDA Inspection, Feb 14, 2019

Record Details

This FDA Inspection record concerns Biomet U.K., Ltd., with an inspection on February 14, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Biomet U.K., Ltd.
Inspection Date: February 14, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Rosanna M. Goodrich (FDA Associated Person)

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ID · e2638e2b-51ac-46ac-af16-c79752c152ef

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1085654
FDA center: Medical Devices & Rad Health
Project area: Postmarket Assurance: Devices
Outcome: Form 483 issued

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FDA Inspection

Biomet U.K., Ltd.February 14, 2019