FDA inspection

Immunodiagnostic Systems Limited: FDA inspection ending Jan 10, 2019

FDA inspection 1094823 · Voluntary Action Indicated (VAI) · Boldon Colliery

Key facts

Inspection ID 1094823
Firm Immunodiagnostic Systems Limited
FEI number 3002485711
Address 10 Didcot Way
City Boldon Colliery
Fiscal year 2019
Inspection end date Jan 10, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical 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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