Form 483

Cenova AB Form 483, 2025-05-08

FDA issued a Form 483 to Cenova AB on 2025-05-08 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Cenova AB · Mjolby, Sweden · Issued May 8, 2025

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.

8 May 2025
21 CFR 820.184

DHR content

Cited by Stephen D Eich

8 May 2025
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Stephen D Eich

8 May 2025
21 CFR 820.75(b)

Lack/Inad procedure-Monitoring/Control of Validated Proces

Cited by Stephen D Eich

8 May 2025
21 CFR 820.90(a)

Nonconforming product control

Cited by Stephen D Eich

Inspected site

CACenova ABMjolby, Sweden

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.75(b)Cited across public-safe Form 483 observations1x
21 CFR 820.90(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