FDA inspection

Clearstream Technologies Ltd: FDA inspection ending Nov 27, 2019

FDA inspection 1123497 · Voluntary Action Indicated (VAI) · Enniscorthy

Key facts

Inspection ID 1123497
Firm Clearstream Technologies Ltd
FEI number 3008906816
Address 19 Commodore Barry Park
City Enniscorthy
Fiscal year 2020
Inspection end date Nov 27, 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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