FDA inspection

The Ritedose Corporation: FDA inspection ending Sep 14, 2007

FDA inspection 488615 · Voluntary Action Indicated (VAI) · Columbia, SC

Key facts

Inspection ID 488615
Firm The Ritedose Corporation
FEI number 3001237796
Address 1 Technology Cir
City Columbia
State SC
ZIP 29203-9591
Fiscal year 2007
Inspection end date Sep 14, 2007
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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
  • 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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