# FDA Inspection 1258920 - BioLife Plasma Services - January 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/biolife-plasma-services/13aca196-afa8-40cc-873b-275fe777d9ec
Source feed: FDA_Inspections

> FDA Inspection 1258920 for BioLife Plasma Services on January 16, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258920
- Company Name: BioLife Plasma Services
- Inspection Date: 2025-01-16
- 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 1258920 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services/99bf6d40-d24b-4714-999c-5d5305dd4a1c)
- [FDA Inspection 1080662 - 2019-02-06](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services/3a777f04-731d-461d-9c18-409e491d7822)

Company: https://www.keypedia.com/companies/biolife-plasma-services/02acc898-d89a-4292-b0ad-adcb4547d979

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