FDA inspection

Catalyst NNG a division of Dynamite Marketing: FDA inspection ending Oct 5, 1999

FDA inspection 651 · Voluntary Action Indicated (VAI) · Urbandale, IA

Key facts

Inspection ID 651
Firm Catalyst NNG a division of Dynamite Marketing
FEI number 1914371
Address 10100 Douglas Ave
City Urbandale
State IA
ZIP 50322-2007
Fiscal year 2000
Inspection end date Oct 5, 1999
Classification Voluntary Action Indicated (VAI)
Project area Monit of Marketed Animal Drug,Feed &Dev
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

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