# FDA Inspection 1045460 - OmniCell, Inc. - February 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/omnicell-inc/02dd349c-5035-4081-ba2e-e9cebc239b1e
Source feed: FDA_Inspections

> FDA Inspection 1045460 for OmniCell, Inc. on February 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1045460
- Company Name: OmniCell, Inc.
- Inspection Date: 2018-02-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1045460 - 2018-02-27](https://www.keypedia.com/records/fda_inspections/omnicell-inc/3e3b5c7c-f4bc-454a-988c-57ce23bf18b8)

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

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