FDA Inspection 1045459 — Omnicell, Inc.

Omnicell, Inc. — FEI 3007880912

The FDA completed an inspection of Omnicell, Inc. on February 27, 2018 in Cranberry Township, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Cranberry Township, PA (United States)