FDA-Inspected Site

Rechon Life Science AB

11 FDA inspections are on record for Rechon Life Science AB in Limhamn, Sweden.

483· Form 483 issued

Limhamn, Sweden · Last updated August 15, 2026

Overview

  • 11 FDA inspections are on record.
  • 7 inspections produced a Form 483.
  • The most recent recorded inspection date is 2024-09-06.

At a glance

Inspections

11

Form 483s

7

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
26 Aug 2024 – 6 Sep 2024Human DrugsWLOn file
9 Mar 2023 – 17 Mar 2023Human Drugs483On file
25 Nov 2019 – 27 Nov 2019Human DrugsClean
25 Jun 2018 – 29 Jun 2018Human Drugs483On file
31 May 2016 – 2 Jun 2016Medical Devices & Rad HealthClean
25 Apr 2016 – 29 Apr 2016Human Drugs483On file
13 Mar 2014 – 21 Mar 2014Human Drugs483On file
16 Sep 2011Not recorded483On file
8 Apr 2008Not recorded483On file
18 Mar 2004Not recordedClean
23 May 2001Not recordedClean

Investigators

FDA investigators tied to this site in the record.

Full site report

Get the verbatim findings behind Rechon Life Science AB's 7 Form 483s

The full inspection record, as Atlas holds it, 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