# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/3bede3a8-f0a2-48ef-b347-97be6af1ffc8

> Inspection records and compliance data for Vitalant in Farmington, New Mexico. Access full analysis and detailed observations.

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## Details

- Name: Vitalant
- FEI Number: 3001487806
- City: Farmington
- State: New Mexico
- Country Name: United States
- Address Line 1: 475 E 20th St Ste A
- Zip Code: 87401

## Related Documents

- [FDA Inspection 1251497 - Vitalant - 2024-08-05](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/a7cd1b95-ad09-4c7f-9546-974b4dad6f15) — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2024
- [FDA Inspection 1118248 - Vitalant - 2020-01-13](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/0c452dc1-d726-439e-9c58-6d6794b8ceec) — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2020
- [FDA Inspection 1049007 - Vitalant - 2018-03-01](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/41e49bd2-80b6-4ca0-a100-e70bd0d2980c) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2018
- [FDA Inspection 967568 - Vitalant - 2016-03-16](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/1895dbfd-99e6-44c0-ae81-a5ccd1201feb) — classification: No Action Indicated (NAI), source: FDA, date: March 16, 2016
- [FDA Inspection 806065 - Vitalant - 2012-10-04](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/dd665260-2f57-4482-ac71-8a7fccd7eb9d) — classification: No Action Indicated (NAI), source: FDA, date: October 4, 2012
- [FDA Inspection 703493 - Vitalant - 2010-12-15](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/67a5bd57-648a-4760-aa29-73a7bb952262) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2010
- [FDA Inspection 582302 - Vitalant - 2009-05-13](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/04fc8434-5091-46fa-9485-a378cb97e026) — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2009

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