# FDA Inspection 1281750 - Vitalant - August 29, 2025

Source: https://www.keypedia.com/records/fda_inspections/vitalant/4828ff80-6984-40e3-99a4-0ad4117b9f84
Source feed: FDA_Inspections

> FDA Inspection 1281750 for Vitalant on August 29, 2025. Classification: N/A.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1281750
- Company Name: Vitalant
- Inspection Date: 2025-08-29
- Product Type: Biologics
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1281750 - 2025-08-29](https://www.keypedia.com/records/fda_inspections/vitalant/ae29ad84-6e79-4024-92d2-f7c31489fdac)
- [FDA Inspection 1167691 - 2022-04-12](https://www.keypedia.com/records/fda_inspections/vitalant/0dec7246-f406-4278-9785-d31a3aaa8b02)
- [FDA Inspection 1167691 - 2022-04-12](https://www.keypedia.com/records/fda_inspections/vitalant/74a42180-2e05-4740-ad33-77c4778528dd)
- [FDA Inspection 1037711 - 2017-12-07](https://www.keypedia.com/records/fda_inspections/vitalant/e5858cea-4756-40ce-a86f-7966ad078532)
- [FDA Inspection 979707 - 2016-07-21](https://www.keypedia.com/records/fda_inspections/vitalant/f36cee3d-ef3f-408f-aafd-90254b894f36)

Company: https://www.keypedia.com/companies/vitalant/f05cb944-4412-45b4-9314-3b7733e6379b

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d