FDA Inspection 1323790 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3030554744

The FDA completed an inspection of BioLife Plasma Services L.P. on Jun 25, 2026 in Thornton, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 25, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Thornton, CO (United States)

Citations

IDCFRDescription
4121 CFR 606.40(a)(1)Provide space for examination
6121 CFR 606.60(a)Provide proper equipment to meet requirements

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.