FDA inspection

Grifols Therapeutics LLC: FDA inspection ending Jan 13, 2011

FDA inspection 710839 · Voluntary Action Indicated (VAI) · Clayton, NC

Key facts

Inspection ID 710839
Firm Grifols Therapeutics LLC
FEI number 1050373
Address 8368 Us 70 Bus Hwy W
City Clayton
State NC
ZIP 27520
Country United States
Fiscal year 2011
Inspection end date Jan 13, 2011
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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