FDA Inspection 712341 — Horiba Instruments Incorporated
The FDA completed an inspection of Horiba Instruments Incorporated on February 7, 2011 in Irvine, CA. 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 7, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Irvine, CA (United States)