FDA inspection

Qiagen Manchester Ltd.: FDA inspection ending Nov 10, 2022

FDA inspection 1199453 · Voluntary Action Indicated (VAI) · Manchester

Key facts

Inspection ID 1199453
Firm Qiagen Manchester Ltd.
FEI number 3009391812
Address St. Marys Hospital, Citylabs 2.0; Hathersage Road
City Manchester
Country United Kingdom
Fiscal year 2023
Inspection end date Nov 10, 2022
Classification Voluntary Action Indicated (VAI)
Project area Project Evaluation: 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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