# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/65b12f4b-9832-4e77-a1e8-ac3c1db9b548

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

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## Details

- Name: Vitalant
- FEI Number: 2970045
- City: Fairfield
- State: California
- Country Name: United States
- Address Line 1: 1325 Gateway Blvd, C-1
- Zip Code: 94533

## Related Documents

- [FDA Inspection 1119506 - Vitalant - 2020-02-12](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/4d319c4d-f9a7-4a4b-be27-b7599164eec5) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2020
- [FDA Inspection 1059979 - Vitalant - 2018-07-09](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/92435101-58a5-4e19-92cb-e5b0466d493d) — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2018
- [FDA Inspection 975889 - Vitalant - 2016-06-29](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/9889446b-3418-44d9-8f5e-ead2b6dace64) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2016
- [FDA Inspection 893478 - Vitalant - 2014-08-27](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/816d50f3-db03-41b7-a75a-68790f2d6a8f) — classification: No Action Indicated (NAI), source: FDA, date: August 27, 2014
- [FDA Inspection 805111 - Vitalant - 2012-10-19](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/cd1dc2d6-c7eb-4489-926a-9b66351fe677) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 19, 2012
- [FDA Inspection 728549 - Vitalant - 2011-06-08](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/df8ee4ae-a208-4171-bc4b-8ba17069c334) — classification: No Action Indicated (NAI), source: FDA, date: June 8, 2011
- [FDA Inspection 577791 - Vitalant - 2009-04-23](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/e8ced131-dc87-470c-ad67-04ce4e28b48b) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2009

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