# FDA Inspection 1031336 - Westone Laboratories, Inc. - November 15, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/westone-laboratories-inc/d7062be9-1d5c-4934-aabb-5c95e309edd2
Source feed: FDA_Inspections

> FDA Inspection 1031336 for Westone Laboratories, Inc. on November 15, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031336
- Company Name: Westone Laboratories, Inc.
- Inspection Date: 2017-11-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1031336 - 2017-11-15](https://www.globalkeysolutions.net/records/fda_inspections/westone-laboratories-inc/1d633c1c-c2c4-4012-8943-3fc03566752c)
- [FDA Inspection 814099 - 2013-01-14](https://www.globalkeysolutions.net/records/fda_inspections/westone-laboratories-inc/4e9f2e32-d917-4412-9430-be6c52feb648)
- [FDA Inspection 814099 - 2013-01-14](https://www.globalkeysolutions.net/records/fda_inspections/westone-laboratories-inc/85adc80b-3e17-482a-8223-c744d3dc8b55)
- [FDA Inspection 790503 - 2012-07-12](https://www.globalkeysolutions.net/records/fda_inspections/westone-laboratories-inc/64252cbb-577c-449d-8a78-11d060ec7bf6)
- [FDA Inspection 790503 - 2012-07-12](https://www.globalkeysolutions.net/records/fda_inspections/westone-laboratories-inc/65257697-930a-4ce2-9d96-1470fa082e32)

Company: https://www.globalkeysolutions.net/companies/westone-laboratories-inc/7a40b1c8-9133-4d76-a102-0d88ae07f7ae

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7