# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/f3791971-06d3-4131-a10f-a89bba9e3c29

> Inspection records and compliance data for Vitalant in Redding, California. Access full analysis and detailed observations.

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## Details

- Name: Vitalant
- FEI Number: 1000522886
- City: Redding
- State: California
- Country Name: United States
- Address Line 1: 2680 Larkspur Ln
- Zip Code: 96002

## Related Documents

- [FDA Inspection 1261748 - Vitalant - 2025-02-12](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/47cd0595-512c-4cba-9a3f-5e47412015fe) — source: FDA, date: February 12, 2025
- [FDA Inspection 1261748 - Vitalant - 2025-02-12](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/682ffc46-ab7f-4ffa-b642-8a1c538acfcd) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2025
- [FDA Inspection 1095064 - Vitalant - 2019-05-30](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/29de2570-c817-47c0-accc-6e16c7848153) — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2019
- [FDA Inspection 1019097 - Vitalant - 2017-07-20](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/c4eb3d2d-4fa7-4c4b-befd-de7aa899ec74) — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2017
- [FDA Inspection 900974 - Vitalant - 2014-10-22](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/2359e8df-cbb3-4b30-bf2b-30d836abf3e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2014
- [FDA Inspection 829293 - Vitalant - 2013-04-23](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/ded2abe7-935d-4201-a7d7-8a3c23dfdf41) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2013
- [FDA Inspection 726389 - Vitalant - 2011-05-20](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/e123fe3b-4c69-48b0-9123-5fb4e430f2ea) — classification: No Action Indicated (NAI), source: FDA, date: May 20, 2011

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