FDA Inspection 1229036 - OmniCell, Inc. - February 01, 2024

FDA Inspection 1229036 for OmniCell, Inc. on February 01, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1229036 for OmniCell, Inc. on February 01, 2024. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

OmniCell, Inc.

Inspection Date

February 1, 2024

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdc44ada-cf0c-4c6f-a35e-722a5f34b0ff

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