# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/be9f6ee8-7471-4a32-896a-426ed550e7f6

> Inspection records and compliance data for Vitalant in Coeur D Alene, Idaho. Access full analysis and detailed observations.

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## Details

- Name: Vitalant
- FEI Number: 3001831403
- City: Coeur D Alene
- State: Idaho
- Country Name: United States
- Address Line 1: 405 W Neider Ave Ste 102
- Zip Code: 83815

## Related Documents

- [FDA Inspection 1256346 - Vitalant - 2024-11-13](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/7e16db93-b862-485d-b8c5-793a429aba3f) — source: FDA, date: November 13, 2024
- [FDA Inspection 1256346 - Vitalant - 2024-11-13](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/ff58b25c-7306-4ba2-b362-11c73088f2c4) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2024
- [FDA Inspection 1098186 - Vitalant - 2019-06-24](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/b1930c0f-df17-4021-b30e-887cb6f702ff) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2019
- [FDA Inspection 925827 - Vitalant - 2015-05-11](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/6d5c976b-8bf8-4eb6-a8f1-7151bd948f13) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2015
- [FDA Inspection 828029 - Vitalant - 2013-04-17](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/6bc4d130-cbae-4b39-9675-c883d9cba194) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2013
- [FDA Inspection 744380 - Vitalant - 2011-09-07](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/09b96969-d32c-48e7-a56a-af4c4efcebd0) — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2011
- [FDA Inspection 552474 - Vitalant - 2008-11-28](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/26ae76ae-a8f2-45ac-8ee3-269fe091b989) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2008

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