FDA inspection

Kaytee Products Inc: FDA inspection ending Aug 26, 2003

FDA inspection 290538 · No Action Indicated (NAI) · Rialto, CA

Key facts

Inspection ID 290538
Firm Kaytee Products Inc
FEI number 2025018
Address 201 S Cactus Ave
City Rialto
State CA
ZIP 92376-6318
Fiscal year 2003
Inspection end date Aug 26, 2003
Classification No Action Indicated (NAI)
Project area Monit of Marketed Animal Drug,Feed &Dev
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

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