FDA Inspection 1197893 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3014353581

The FDA completed an inspection of BioLife Plasma Services L.P. on Jan 26, 2023 in Cordova, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 26, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Cordova, TN (United States)

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