FDA Inspection 779779 — BPL Plasma Inc

BPL Plasma Inc — FEI 2475932

The FDA completed an inspection of BPL Plasma Inc on May 4, 2012 in Queens Village, NY. 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
May 4, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Queens Village, NY (United States)

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