FDA inspection

Qiagen Manchester Ltd.: FDA inspection ending Sep 12, 2013

FDA inspection 853010 · No Action Indicated (NAI) · Manchester

Key facts

Inspection ID 853010
Firm Qiagen Manchester Ltd.
FEI number 3009391812
Address CityLabs 2.0, Hathersage Road
City Manchester
Country United Kingdom
Fiscal year 2013
Inspection end date Sep 12, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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