Form 483

Fresenius Medical Care Holdings, Inc. Form 483, 2024-10-16

FDA issued a Form 483 to Fresenius Medical Care Holdings, Inc. on 2024-10-16 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Fresenius Medical Care Holdings, Inc. · Waltham, United States · Issued October 16, 2024

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

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

16 Oct 2024
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Sunita Pandey

16 Oct 2024
21 CFR 820.30(g)

Design Validation - Risk analysis not performed/inadequate

Cited by Sunita Pandey

16 Oct 2024
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Sunita Pandey

16 Oct 2024
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Sunita Pandey

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.30(i)Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, 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