FDA inspection

BioLife Plasma Services L.P.: FDA inspection ending Oct 5, 2012

FDA inspection 802348 · No Action Indicated (NAI) · Ames, IA

Key facts

Inspection ID 802348
Firm BioLife Plasma Services L.P.
FEI number 3001629960
Address 1618 Golden Aspen Dr
City Ames
State IA
ZIP 50010
Country United States
Fiscal year 2013
Inspection end date Oct 5, 2012
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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