FDA Inspection 579412 — Westone Laboratories, Inc.
The FDA completed an inspection of Westone Laboratories, Inc. on Apr 6, 2009 in Colorado Springs, CO. 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
- Apr 6, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Colorado Springs, CO (United States)