FDA inspection

Diazyme Laboratories: FDA inspection ending Nov 9, 2005

FDA inspection 401732 · Official Action Indicated (OAI) · Poway, CA

Key facts

Inspection ID 401732
Firm Diazyme Laboratories
FEI number 3004445302
Address 12889 Gregg Ct
City Poway
State CA
ZIP 92064-6833
Fiscal year 2006
Inspection end date Nov 9, 2005
Classification Official Action Indicated (OAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • 10–99 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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