# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/53210f12-3fe2-4006-a446-a8f926583960

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

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## Details

- Name: Vitalant
- FEI Number: 3003609162
- City: Elk Grove
- State: California
- Country Name: United States
- Address Line 1: 9267 Laguna Springs Dr Ste 100
- Zip Code: 95758

## Related Documents

- [FDA Inspection 1247163 - Vitalant - 2024-08-07](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/f300122d-3b5f-4420-8224-64f4b3e47fc9) — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2024
- [FDA Inspection 1076433 - Vitalant - 2018-11-27](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/5e8973ea-735c-46d1-a7f5-511f3a24d28e) — classification: No Action Indicated (NAI), source: FDA, date: November 27, 2018
- [FDA Inspection 999732 - Vitalant - 2016-12-07](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/ffdde8ad-6f10-4cf7-bd45-3fcb62cc68be) — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2016
- [FDA Inspection 911710 - Vitalant - 2015-01-14](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/04ff9416-e609-479c-87d3-9fc1890d26e3) — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2015
- [FDA Inspection 810328 - Vitalant - 2012-12-12](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/668d7ef0-366a-404e-b9cc-7e445d80f48e) — classification: No Action Indicated (NAI), source: FDA, date: December 12, 2012
- [FDA Inspection 720616 - Vitalant - 2011-04-19](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/2b4263ce-c734-4d51-ac0f-b9bcb4f4f46e) — classification: No Action Indicated (NAI), source: FDA, date: April 19, 2011
- [FDA Inspection 620103 - Vitalant - 2009-06-02](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/b6006f7e-1214-4ec7-a2a9-5c845c861cfa) — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2009

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