# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/5fe671a6-936f-4667-b564-401b574f2409

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

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## Details

- Name: Vitalant
- FEI Number: 1000112530
- City: Southaven
- State: Mississippi
- Country Name: United States
- Address Line 1: 1055 Goodman Rd E Ste J
- Zip Code: 38671

## Related Documents

- [FDA Inspection 1226509 - Vitalant - 2023-12-18](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/02d7dfc1-0267-4feb-a104-5c8b90bbfd14) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2023
- [FDA Inspection 1091225 - Vitalant - 2019-05-08](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/6ff3f01c-d67a-4256-b166-6964f3e52f8a) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2019
- [FDA Inspection 1006995 - Vitalant - 2017-03-28](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/901e9c90-9fc5-4532-adf7-c70cee20c318) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2017
- [FDA Inspection 938405 - Vitalant - 2015-08-06](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/90495b30-4496-4e89-b49f-1e0b11f0bea2) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2015
- [FDA Inspection 837426 - Vitalant - 2013-06-20](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/fd089f5b-ef4d-44b2-83c9-e3434a57a4ab) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2013
- [FDA Inspection 729747 - Vitalant - 2011-06-07](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/ea501b24-4be3-4ef0-8574-a69fda019265) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2011
- [FDA Inspection 589084 - Vitalant - 2009-06-05](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/06daf65a-12e9-4c98-9846-6114d2954b23) — classification: No Action Indicated (NAI), source: FDA, date: June 5, 2009

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