# FDA Inspection 1259448 - Vitalant - January 24, 2025

Source: https://www.keypedia.com/records/fda_inspections/vitalant/48e8746f-dcab-4185-92f3-71208a21ef34
Source feed: FDA_Inspections

> FDA Inspection 1259448 for Vitalant on January 24, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259448
- Company Name: Vitalant
- Inspection Date: 2025-01-24
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1259448 - 2025-01-24](https://www.keypedia.com/records/fda_inspections/vitalant/96f05a22-26f7-4742-b49e-e4b8a4086f95)
- [FDA Inspection 1142856 - 2021-05-18](https://www.keypedia.com/records/fda_inspections/vitalant/50fd18f6-8dc8-4953-b03d-b6d1110d5b59)
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- [FDA Inspection 1056338 - 2018-06-07](https://www.keypedia.com/records/fda_inspections/vitalant/ad2260aa-cd14-409a-8904-43c82f6031d3)
- [FDA Inspection 972547 - 2016-05-25](https://www.keypedia.com/records/fda_inspections/vitalant/850341e4-bbfd-477f-b90f-b33f5ee2d664)

Company: https://www.keypedia.com/companies/vitalant/e458c753-02f1-438a-af41-f923b545fb12

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d
