FDA Inspection 903156 — Guidewire Technologies, Inc.
The FDA completed an inspection of Guidewire Technologies, Inc. on Nov 19, 2014 in Salem, NH. 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
- Nov 19, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Salem, NH (United States)