FDA inspection

The Ritedose Corporation: FDA inspection ending Sep 9, 2011

FDA inspection 744752 · No Action Indicated (NAI) · Columbia, SC

Key facts

Inspection ID 744752
Firm The Ritedose Corporation
FEI number 3001237796
Address 1 Technology Cir
City Columbia
State SC
ZIP 29203
Country United States
Fiscal year 2011
Inspection end date Sep 9, 2011
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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