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 July 10, 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.

Jose A Cruz Gonzalez2 insp.
Amir Alavi1 insp.
MRA DavisM1 insp.
Frederick Razzaghi1 insp.
Akbar J Zaidi1 insp.
Russell J Glapion1 insp.
Helen B Ricalde1 insp.
Tiffani D Wilson1 insp.

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

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