FDA inspection

Integris Baptist Medical Center IRB: FDA inspection ending Sep 17, 2008

FDA inspection 537354 · No Action Indicated (NAI) · Oklahoma City, OK

Key facts

Inspection ID 537354
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 2008
Inspection end date Sep 17, 2008
Classification No Action Indicated (NAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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