FDA inspection

Woodward Iodine Corporation: FDA inspection ending Sep 1, 2005

FDA inspection 393782 · Voluntary Action Indicated (VAI) · Woodward, OK

Key facts

Inspection ID 393782
Firm Woodward Iodine Corporation
FEI number 1626455
Address 8 Mi North Hwy 34,3 Miles East EW-32, Po Box 1245
City Woodward
State OK
ZIP 73802-1245
Fiscal year 2005
Inspection end date Sep 1, 2005
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
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
  • 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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