FDA-Inspected Site

Pentapharm Ag

2 FDA inspections are on record for Pentapharm Ag in Aesch BL, Switzerland.

483· Form 483 issued

Aesch BL, Switzerland · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2016-09-15.

At a glance

Inspections

2

Form 483s

1

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
12 Sep 2016 – 15 Sep 2016Medical Devices & Rad Health483View 483 →
17 Feb 2014 – 20 Feb 2014Human DrugsClean

Observations on record

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

15 Sep 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Marissa S Steinhagen

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

Full site report

Get the verbatim findings behind Pentapharm Ag's 1 Form 483

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