FDA Inspection 946183 — Agilent Technologies, Inc.
The FDA completed an inspection of Agilent Technologies, Inc. on Oct 23, 2015 in Carpinteria, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 23, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Carpinteria, CA (United States)