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

Source: https://www.globalkeysolutions.net/records/fda_inspections/omnicell-inc/fdc44ada-cf0c-4c6f-a35e-722a5f34b0ff/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1229036
- Company Name: OmniCell, Inc.
- Inspection Date: 2024-02-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1045460 - 2018-02-27](https://www.globalkeysolutions.net/api/records/fda_inspections/omnicell-inc/3e3b5c7c-f4bc-454a-988c-57ce23bf18b8/)
- [FDA Inspection 1045460 - 2018-02-27](https://www.globalkeysolutions.net/api/records/fda_inspections/omnicell-inc/02dd349c-5035-4081-ba2e-e9cebc239b1e/)

Company: https://www.globalkeysolutions.net/companies/omnicell-inc/2a40261b-6bed-411e-89b2-fd1c1ec8e41e

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7