FDA inspection

ARL Biopharma, Inc. dba Analytical Research Laboratories: FDA inspection ending Aug 17, 2007

FDA inspection 486613 · No Action Indicated (NAI) · Oklahoma City, OK

Key facts

Inspection ID 486613
Firm ARL Biopharma, Inc. dba Analytical Research Laboratories
FEI number 3003644883
Address 840 Research Pkwy Ste 546
City Oklahoma City
State OK
ZIP 73104-3697
Fiscal year 2007
Inspection end date Aug 17, 2007
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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

Browse all FDA inspections