FDA Inspection 947392 — Agilent Technologies, Inc.
The FDA completed an inspection of Agilent Technologies, Inc. on Oct 23, 2015 in Carpinteria, CA. 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
- Oct 23, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Carpinteria, CA (United States)
Additional Details
Sponsor, Contract Research Organization