FDA Inspection 1106696 — BioLife Plasma Services L.P.

BioLife Plasma Services L.P. — FEI 3010960208

The FDA completed an inspection of BioLife Plasma Services L.P. on October 17, 2019 in Grandville, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 17, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grandville, MI (United States)

Citations

IDCFRDescription
442521 CFR 606.60(a)Equipment observed, standardized, calibrated