FDA-Inspected Site

Cepheid Ab

2 FDA inspections are on record for Cepheid Ab in Solna, Sweden.

Clean· No action indicated

Solna, Sweden · Last updated July 9, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2017-03-15.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
13 Mar 2017 – 15 Mar 2017Medical Devices & Rad HealthClean
30 Mar 2015 – 31 Mar 2015Medical Devices & Rad HealthWLView 483 →

Observations on record

Form 483 observations cited at this site, most recent first.

31 Mar 2015
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Dorothy W Lee

31 Mar 2015
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Dorothy W Lee

31 Mar 2015
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Dorothy W Lee

31 Mar 2015
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Dorothy W Lee

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.30(i)Cited across public-safe Form 483 observations1x
21 CFR 820.50Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Cepheid Ab's 1 Form 483

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat