FDA inspection

OneBlood, Inc.: FDA inspection ending May 9, 2018

FDA inspection 1054607 · No Action Indicated (NAI) · New Port Richey, FL

Key facts

Inspection ID 1054607
Firm OneBlood, Inc.
FEI number 1035903
Address 5355 Us Highway 19
City New Port Richey
State FL
ZIP 34652
Country United States
Fiscal year 2018
Inspection end date May 9, 2018
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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