# Vitalant, Spokane, WA – FDA Inspections

Source: https://www.keypedia.com/companies/vitalant/7a5079bf-12d6-460a-b20d-eacf8b0f3f11

> Inspection records and compliance data for Vitalant in Spokane, Washington. 7 FDA inspections on record, 1 Form 483, last inspected November 22, 2024.

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## Details

- Name: Vitalant
- FEI Number: 3071345
- Address Line 1: 210 W Cataldo Ave
- City: Spokane
- State: Washington
- Zip Code: 99201
- Country Name: United States
- Address: 210 W Cataldo Ave, Spokane, Washington 99201, United States
- Country: United States

## Related Documents

- FDA Inspection 1258010 - Vitalant - 2024-11-22 — source: FDA, date: November 22, 2024
- [FDA Inspection 1258010 - Vitalant - 2024-11-22](https://www.keypedia.com/records/fda_inspections/vitalant/ef531390-28ec-4538-840b-31ea72884326) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2024
- FDA Inspection 1106275 - Vitalant - 2019-09-05 — classification: No Action Indicated (NAI), source: FDA, date: September 5, 2019
- [FDA Inspection 1000905 - Vitalant - 2017-02-10](https://www.keypedia.com/records/fda_inspections/vitalant/16457b79-8da2-405e-8b06-7a324482a026) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2017
- FDA Inspection 937619 - Vitalant - 2015-07-29 — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2015
- [FDA Inspection 848182 - Vitalant - 2013-09-13](https://www.keypedia.com/records/fda_inspections/vitalant/5be7f3d8-d2f0-469e-bae3-e9abd3f4563d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2013
- [FDA Inspection 795373 - Vitalant - 2012-08-15](https://www.keypedia.com/records/fda_inspections/vitalant/4e0d2829-72dc-49b1-8fcf-12d2ff488c7f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 15, 2012
- [FDA Inspection 675546 - Vitalant - 2010-07-21](https://www.keypedia.com/records/fda_inspections/vitalant/a7230f10-48f2-47a6-863f-f71646b32000) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2010

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