FDA-Inspected Site

Dermeo

1 FDA inspection is on record for Dermeo in Paris, France.

483· Form 483 issued

Paris, France · Last updated July 10, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2016-04-28.

At a glance

Inspections

1

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
25 Apr 2016 – 28 Apr 2016Medical Devices & Rad Health483View 483 →

Observations on record

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

28 Apr 2016
21 CFR 820.198(c)

Investigation of device failures

Cited by Thai T Duong, Amanda S Zorn

28 Apr 2016
21 CFR 820.198(c)

Investigation of device failures

Cited by Thai T Duong, Amanda S Zorn

28 Apr 2016
21 CFR 820.30(g)

Design validation - software validation not performed

Cited by Thai T Duong, Amanda S Zorn

28 Apr 2016
21 CFR 820.90(a)

Nonconforming product control

Cited by Thai T Duong, Amanda S Zorn

28 Apr 2016
21 CFR 820.90(a)

Nonconforming product control

Cited by Thai T Duong, Amanda S Zorn

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 820.198(c)Cited across public-safe Form 483 observations3x
21 CFR 820.30(g)Cited across public-safe Form 483 observations3x
21 CFR 820.90(a)Cited across public-safe Form 483 observations3x

Full site report

Get the verbatim findings behind Dermeo'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