FDA Inspection
Westone Laboratories, Inc.Westone Laboratories, Inc. – FDA Inspection, Jul 12, 2012
Record Details
This FDA Inspection record concerns Westone Laboratories, Inc., with an inspection on July 12, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Westone Laboratories, Inc.
- Inspection Date
- July 12, 2012
- Product Type
- Devices
View Company Profile
ID · 64252cbb-577c-449d-8a78-11d060ec7bf6
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 790503
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Westone Laboratories, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 15, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 14, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 6, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Westone Laboratories, Inc.
- FDA Inspection 1031336 - 2017-11-15
- FDA Inspection 814099 - 2013-01-14
- FDA Inspection 579412 - 2009-04-06
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.