Form 483

Miele & Cie. KG Form 483, 2018-04-19

FDA issued a Form 483 to Miele & Cie. KG on 2018-04-19 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

Miele & Cie. KG · Oelde, Germany · Issued April 19, 2018

Overview

  • 3 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.

19 Apr 2018
21 CFR 1010.2(c)

Certification not based on adequate test/testing program

Cited by Gregory M Bessette, Michael P Sweeney

19 Apr 2018
21 CFR 1030.10(c)(3)(i)

tests--errors and uncertainties accounted for

Cited by Gregory M Bessette, Michael P Sweeney

19 Apr 2018
21 CFR 1030.10(c)(3)(iii)

Measurements with tap water container

Cited by Gregory M Bessette, Michael P Sweeney

Inspected site

M&Miele & Cie. KGOelde, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1010.2(c)Cited across public-safe Form 483 observations1x
21 CFR 1030.10(c)(3)(i)Cited across public-safe Form 483 observations1x
21 CFR 1030.10(c)(3)(iii)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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