FDA Inspection 1045460 — OmniCell, Inc.
The FDA completed an inspection of OmniCell, Inc. on Feb 27, 2018 in Warrendale, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 27, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Warrendale, PA (United States)