Form 483

Dermeo Form 483, 2016-04-28

FDA issued a Form 483 to Dermeo on 2016-04-28 with 9 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health9 observations

Dermeo · Paris, France · Issued April 28, 2016

Overview

  • 9 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

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

Inspected site

DDermeoParis, France

Inspection team

Cited regulations

CFR citations associated with this Form 483.

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 483 report

Get the verbatim text of all 9 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere