FDA inspection

IND Diagnostic Inc.: FDA inspection ending Jul 22, 2005

FDA inspection 388043 · Official Action Indicated (OAI) · Delta

Key facts

Inspection ID 388043
Firm IND Diagnostic Inc.
FEI number 3003148151
Address 1629 Foster's Way
City Delta
Fiscal year 2005
Inspection end date Jul 22, 2005
Classification Official Action Indicated (OAI)
Project area Product Evaluation: Med Devices
Product type Devices

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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