Form 483

Diagnostic Grifols, S.A. Form 483, 2017-02-16

FDA issued a Form 483 to Diagnostic Grifols, S.A. on 2017-02-16 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Diagnostic Grifols, S.A. · Parets Del Valles, Spain · Issued February 16, 2017

Overview

  • 6 public-safe observations are available for this inspection.
  • 3 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 Feb 2017
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Roy Baby

16 Feb 2017
21 CFR 820.250(b)

Sampling plans

Cited by Roy Baby

16 Feb 2017
21 CFR 820.250(b)

Sampling plans

Cited by Roy Baby

16 Feb 2017
21 CFR 820.50(a)(1)

Evaluation and Selection, Suppliers, Contractors, etc.

Cited by Roy Baby

16 Feb 2017
21 CFR 803.50(a)(2)

Report of Malfunction

Cited by Roy Baby

Inspected site

DGDiagnostic Grifols, S.A.Parets Del Valles, Spain

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(2)Cited across public-safe Form 483 observations2x
21 CFR 820.250(b)Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)(1)Cited across public-safe Form 483 observations2x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 6 observations

The source PDF and 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