FDA inspection

Integris Baptist Medical Center IRB: FDA inspection ending Jan 9, 2003

FDA inspection 255524 · Voluntary Action Indicated (VAI) · Oklahoma City, OK

Key facts

Inspection ID 255524
Firm Integris Baptist Medical Center IRB
FEI number 1643747
Address 3400 Northwest Expressway Ste 806
City Oklahoma City
State OK
ZIP 73112-4491
Fiscal year 2003
Inspection end date Jan 9, 2003
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 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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