FDA inspection

BioLife Plasma Services L.P.: FDA inspection ending Aug 25, 2017

FDA inspection 1022840 · Voluntary Action Indicated (VAI) · Greenwood, IN

Key facts

Inspection ID 1022840
Firm BioLife Plasma Services L.P.
FEI number 3012415306
Address 1138 N Emerson Ave
City Greenwood
State IN
ZIP 46143
Country United States
Fiscal year 2017
Inspection end date Aug 25, 2017
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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