FDA Inspection 675235 — PlasmaLab International, Inc.

PlasmaLab International, Inc. — FEI 3023431

The FDA completed an inspection of PlasmaLab International, Inc. on June 16, 2010 in Everett, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 16, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Everett, WA (United States)

Citations

IDCFRDescription
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
924321 CFR 630.40(a)Notification