# Westone Laboratories, Inc., Colorado Springs, CO – FDA Inspections

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

> Inspection records and compliance data for Westone Laboratories, Inc. in Colorado Springs, Colorado. 4 FDA inspections on record (1 OAI), 1 Form 483, last inspected November 15, 2017.

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## Details

- Name: Westone Laboratories, Inc.
- FEI Number: 2094377
- Address Line 1: 2235 Executive Cir
- City: Colorado Springs
- State: Colorado
- Zip Code: 80906
- Country Name: United States
- Address: 2235 Executive Cir, Colorado Springs, Colorado 80906, United States
- Country: United States

## Related Documents

- FDA Inspection 1031336 - Westone Laboratories, Inc. - 2017-11-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2017
- [FDA Inspection 1031336 - Westone Laboratories, Inc. - 2017-11-15](https://www.keypedia.com/records/fda_inspections/westone-laboratories-inc/d7062be9-1d5c-4934-aabb-5c95e309edd2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2017
- FDA Inspection 814099 - Westone Laboratories, Inc. - 2013-01-14 — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2013
- [FDA Inspection 814099 - Westone Laboratories, Inc. - 2013-01-14](https://www.keypedia.com/records/fda_inspections/westone-laboratories-inc/85adc80b-3e17-482a-8223-c744d3dc8b55) — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2013
- [FDA Inspection 790503 - Westone Laboratories, Inc. - 2012-07-12](https://www.keypedia.com/records/fda_inspections/westone-laboratories-inc/64252cbb-577c-449d-8a78-11d060ec7bf6) — classification: Official Action Indicated (OAI), source: FDA, date: July 12, 2012
- FDA Inspection 790503 - Westone Laboratories, Inc. - 2012-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2012
- FDA Inspection 579412 - Westone Laboratories, Inc. - 2009-04-06 — classification: No Action Indicated (NAI), source: FDA, date: April 6, 2009

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