FDA inspection

Cepheid Ab: FDA inspection ending Mar 15, 2017

FDA inspection 1006012 · No Action Indicated (NAI) · Solna

Key facts

Inspection ID 1006012
Firm Cepheid Ab
FEI number 3009613136
Address Rontgenvagen 7
City Solna
Country Sweden
Fiscal year 2017
Inspection end date Mar 15, 2017
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

Browse all FDA inspections