# FDA Inspection 1045459 - Omnicell, Inc. - February 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/omnicell-inc/86abce40-a09f-4e7b-a538-a0fbecdfd197
Source feed: FDA_Inspections

> FDA Inspection 1045459 for Omnicell, Inc. on February 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1045459
- Company Name: Omnicell, Inc.
- Inspection Date: 2018-02-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/omnicell-inc/3a36b6b6-efe6-42d7-83cb-2c55f17cf689

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