FDA Inspection 1320404 — Omnicell, Inc.

Omnicell, Inc. — FEI 3007880912

The FDA completed an inspection of Omnicell, Inc. on May 27, 2026 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
May 27, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Cranberry Township, PA (United States)