FDA inspection

Clearstream Technologies Ltd: FDA inspection ending Jan 31, 2019

FDA inspection 1078231 · Voluntary Action Indicated (VAI) · Enniscorthy

Key facts

Inspection ID 1078231
Firm Clearstream Technologies Ltd
FEI number 3008906816
Address 19 Commodore Barry Park
City Enniscorthy
Country Ireland
Fiscal year 2019
Inspection end date Jan 31, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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