# Westone Laboratories, Inc. – FDA Inspection, Nov 15, 2017

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

> FDA inspection 1031336 of Westone Laboratories, Inc., November 15, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 814099 - 2013-01-14](https://www.keypedia.com/records/fda_inspections/westone-laboratories-inc/85adc80b-3e17-482a-8223-c744d3dc8b55)
- [FDA Inspection 790503 - 2012-07-12](https://www.keypedia.com/records/fda_inspections/westone-laboratories-inc/64252cbb-577c-449d-8a78-11d060ec7bf6)
- FDA Inspection 579412 - 2009-04-06

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/vicky-l-cruz/282da571-56be-48f4-96c6-d590829b12c2)

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

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