# Vitalant - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant/a5d0608c-c3d7-4345-9190-a4a9f391b5c7

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

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## Details

- Name: Vitalant
- FEI Number: 3003832489
- City: Greensburg
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 6044 Route 30 Ste 300
- Zip Code: 15601

## Related Documents

- [FDA Inspection 1238535 - Vitalant - 2024-05-09](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/e3c79028-63ce-4c27-ba30-240b85dcf4e9) — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2024
- [FDA Inspection 1100795 - Vitalant - 2019-07-30](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/a8d4f26e-2721-493c-80d1-012a69be0f1b) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2019
- [FDA Inspection 1000614 - Vitalant - 2017-01-10](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/2b78bc74-ce40-4f09-9bc9-f477ebfca3cd) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2017
- [FDA Inspection 910116 - Vitalant - 2015-01-15](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/d4aa5cc6-a8b7-49d6-8586-81536703f88b) — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2015
- [FDA Inspection 810119 - Vitalant - 2012-11-08](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/3dc365cf-9d39-4bd9-aded-60fde428b898) — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2012
- [FDA Inspection 699289 - Vitalant - 2010-11-23](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/1c45e785-c856-4c61-8704-52cecd1a779f) — classification: No Action Indicated (NAI), source: FDA, date: November 23, 2010
- [FDA Inspection 567903 - Vitalant - 2009-03-05](https://www.globalkeysolutions.net/records/fda_inspections/vitalant/599718a1-4578-4632-95de-fb14813de903) — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2009

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