Form 483

Cellpack Ag Form 483, 2014-05-01

FDA issued a Form 483 to Cellpack Ag on 2014-05-01 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Cellpack Ag · Villmergen, Switzerland · Issued May 1, 2014

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

1 May 2014
21 CFR 820.22

Quality audits - auditor independence

Cited by Satheesh Thomas

1 May 2014
21 CFR 820.25(b)

Training records

Cited by Satheesh Thomas

1 May 2014
21 CFR 820.70(b)

Production and Process Change Procedures, lack of or Inad.

Cited by Satheesh Thomas

1 May 2014
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Satheesh Thomas

1 May 2014
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Satheesh Thomas

Inspected site

CACellpack AgVillmergen, Switzerland

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 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.70(b)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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