FDA inspection

The Ritedose Corporation: FDA inspection ending Apr 18, 2019

FDA inspection 1089541 · No Action Indicated (NAI) · Columbia, SC

Key facts

Inspection ID 1089541
Firm The Ritedose Corporation
FEI number 3001237796
Address 1 Technology Cir
City Columbia
State SC
ZIP 29203
Country United States
Fiscal year 2019
Inspection end date Apr 18, 2019
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
Product type Drugs

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

Browse all FDA inspections